Target Name: PICALM
NCBI ID: G8301
Review Report on PICALM Target / Biomarker Content of Review Report on PICALM Target / Biomarker
PICALM
Other Name(s): Clathrin assembly lymphoid myeloid leukemia protein | CALM | phosphatidylinositol binding clathrin assembly protein | PICAL_HUMAN | LAP | CALM/AF10 fusion protein | PICALM variant 1 | Phosphatidylinositol binding clathrin assembly protein, transcript variant 1 | Phosphatidylinositol binding clathrin assembly protein, transcript variant 2 | Phosphatidylinositol-binding clathrin assembly protein (isoform 2) | clathrin assembly lymphoid myeloid leukemia protein | Phosphatidylinositol-binding clathrin assembly protein (isoform 1) | CLTH | PICALM variant 2 | Phosphatidylinositol-binding clathrin assembly protein

Picalm: A Potential Cancer Treatment Target

Picalm is a protein that is expressed in a variety of tissues, including the bone marrow, spleen, and lymph nodes. It is a member of the Clathrin assembly lymphoid myeloid leukemia (CALML) family, which is characterized by the presence of a specific type ofcalbindin protein in the cells. Picalm is a potential drug target or biomarker for the treatment of various types of cancer.

The Picalm Protein

Picalm is a transmembrane protein that is expressed in a variety of tissues throughout the body. It is synthesized using the gene EBF2, which is located on chromosome 17. Picalm consists of four distinct isoforms, which are produced by alternative splicing of the EBF2 gene. These isoforms are characterized by the presence or absence of different amino acid residues at their C-terminus.

The most abundant isoform of Picalm is a 21-kDa protein that is predominantly expressed in the bone marrow. This isoform is composed of a single polypeptide chain that contains the following amino acid residues:

* Asp (21), Glu (21), Lys (21), Asn (22), Asp (23), Lys (23), Isoleucine (24), Leucine (25), Lys (26), Arg (27), Asn (28), Asp (29), Lys (30), Asp (31), Lys (32), Isoleucine (33), Leucine (34), Lys (35), Asp (36), Lys (37), Asp (38), Lys (39), Asp (40), Lys (41), Asp (42), Lys (43), Asp (44), Lys (45), Asp (46), Lys (47), Asp (48), Lys (49), Asp (50), Lys (51), Asp (52), Lys (53), Asp (54), Lys (55), Asp (56), Lys (57), Asp (58), Lys (59), Asp (60), Lys (61), Asp (62), Lys (63), Asp (64), Lys (65), Asp (66), Lys (67), Asp (68), Lys (69), Asp (70), Lys (71), Asp (72), Lys (73), Asp (74), Lys (75), Asp (76), Lys (77), Asp (78), Lys (79), Asp (80), Lys (81), Asp (82), Lys (83), Asp (84), Lys (85), Asp (86), Lys (87), Asp (88), Lys (89), Asp (90), Lys (91), Asp (92), Lys (93), Asp (94), Lys (95), Asp (96), Lys (97), Asp (98), Lys (99), Asp (100), Lys (101), Asp (102), Lys (103), Asp (104), Lys (105), Asp (106), Lys (107), Asp (108), Lys (109), Asp (110), Lys (111), Asp (112), Lys (113), Asp (114), Lys (115), Asp (116), Lys (117), Asp (118), Lys (119), Asp (120), Lys (121), Asp (122), Lys (123), Asp (124), Lys (125), Asp (126), Lys (127), Asp (128), Lys (129), Asp (130), Lys (131), Asp (132), Lys (133), Asp (134), Lys (135), Asp (136), Lys (137), Asp (138), Lys (139), Asp (140), Lys (141), Asp (142), Lys (143), Asp (144), Lys (145), Asp (146), Lys (147), Asp (148), Lys (149), Asp (150), Lys (151), Asp (152), Lys (153), Asp (154), Lys (155), Asp (156), Lys (157), Asp (158), Lys (159), Asp (160), Lys (161), Asp (162), Lys (163), Asp (164), Lys (165), Asp (166), Lys (167), Asp (168), Lys (169), Asp (170), Lys (171), Asp (172), Lys (173), Asp (174), Lys (175), Asp (176), Lys (177), Asp (178), Lys (179), Asp (180), Lys (181), Asp (182), Lys (183), Asp (184), Lys (185), Asp (186), Lys (187), Asp (188), Lys (189), Asp (190), Lys (191), Asp (192), Lys (193), Asp (194), Lys (195), Asp (196), Lys (197), Asp (198), Lys (199), Asp (200), Lys (201), Asp (202), Lys (203), Asp (204), Lys (205), Asp (206), Lys (207), Asp (208), Lys (209), Asp (210), Lys (211), Asp (212), Lys (213), Asp (214), Lys (215), Asp (216), Lys (217), Asp (218), Lys (219), Asp (220), Lys (221), Asp (222), Lys (223), Asp (224), Lys (225), Asp (226), Lys (227), Asp (228), Lys (229), Asp (230), Lys (231), Asp (232), Lys (233), Asp (234), Lys (235), Asp (236), Lys (237), Asp (238), Lys (239), Asp (240), Lys (241), Asp (242), Lys (243), Asp (244), Lys (245), Asp (246), Lys (247), Asp (248), Lys (249), Asp (250), Lys (251), Asp (252), Lys (253), Asp (254), Lys (255), Asp (256), Lys (257), Asp (258), Lys (259), Asp (260), Lys (261), Asp (262), Lys (263), Asp (264), Lys (265), Asp (266), Lys (267), Asp (268), Lys (269), Asp (270), Lys (271), Asp (272), Lys (273), Asp (274), Lys (275), Asp (

Protein Name: Phosphatidylinositol Binding Clathrin Assembly Protein

Functions: Cytoplasmic adapter protein that plays a critical role in clathrin-mediated endocytosis which is important in processes such as internalization of cell receptors, synaptic transmission or removal of apoptotic cells. Recruits AP-2 and attaches clathrin triskelions to the cytoplasmic side of plasma membrane leading to clathrin-coated vesicles (CCVs) assembly (PubMed:10436022, PubMed:16262731, PubMed:27574975). Furthermore, regulates clathrin-coated vesicle size and maturation by directly sensing and driving membrane curvature (PubMed:25898166). In addition to binding to clathrin, mediates the endocytosis of small R-SNARES (Soluble NSF Attachment Protein REceptors) between plasma membranes and endosomes including VAMP2, VAMP3, VAMP4, VAMP7 or VAMP8 (PubMed:22118466, PubMed:21808019, PubMed:23741335). In turn, PICALM-dependent SNARE endocytosis is required for the formation and maturation of autophagic precursors (PubMed:25241929). Modulates thereby autophagy and the turnover of autophagy substrates such as MAPT/TAU or amyloid precursor protein cleaved C-terminal fragment (APP-CTF) (PubMed:25241929, PubMed:24067654)

The "PICALM Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about PICALM comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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