Autophagy, Sorting nexin-4 (ATG24) phosphoinositide-binding
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 4 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005768 | endosome | 7 | 1 |
GO:0012506 | vesicle membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 1 |
GO:0030666 | endocytic vesicle membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IBF2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0006898 | receptor-mediated endocytosis | 6 | 1 |
GO:0006914 | autophagy | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005543 | phospholipid binding | 3 | 12 |
GO:0008289 | lipid binding | 2 | 12 |
GO:0035091 | phosphatidylinositol binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.324 |
CLV_PCSK_FUR_1 | 234 | 238 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.311 |
CLV_PCSK_PC7_1 | 106 | 112 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.582 |
DEG_APCC_DBOX_1 | 109 | 117 | PF00400 | 0.321 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.321 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.321 |
DEG_APCC_DBOX_1 | 408 | 416 | PF00400 | 0.579 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.692 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 225 | 231 | PF00134 | 0.453 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.411 |
DOC_SPAK_OSR1_1 | 149 | 153 | PF12202 | 0.517 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 384 | 388 | PF12436 | 0.306 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 149 | 159 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 208 | 217 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 236 | 245 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 334 | 343 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.418 |
LIG_APCC_ABBA_1 | 372 | 377 | PF00400 | 0.426 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.367 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.453 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.354 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.419 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.373 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.453 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.453 |
LIG_LIR_Apic_2 | 26 | 31 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 369 | 377 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.304 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.306 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.422 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.426 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.426 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.363 |
LIG_SH2_PTP2 | 28 | 31 | PF00017 | 0.496 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.122 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.229 |
LIG_SH3_2 | 144 | 149 | PF14604 | 0.589 |
LIG_SH3_2 | 69 | 74 | PF14604 | 0.306 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.573 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.306 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.395 |
LIG_SUMO_SIM_par_1 | 391 | 396 | PF11976 | 0.426 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.632 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.426 |
LIG_TYR_ITIM | 116 | 121 | PF00017 | 0.426 |
LIG_WW_3 | 146 | 150 | PF00397 | 0.577 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.737 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.453 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.433 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.420 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.573 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.394 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.402 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.321 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.423 |
MOD_Cter_Amidation | 271 | 274 | PF01082 | 0.426 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.698 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.603 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.426 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.339 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.351 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.461 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.327 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.589 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.657 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.510 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.468 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.426 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.402 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.324 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.416 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.418 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.317 |
MOD_LATS_1 | 235 | 241 | PF00433 | 0.453 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.471 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.499 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.384 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.376 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.464 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.394 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.561 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.453 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.374 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.546 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.553 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.605 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.459 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.426 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.321 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.391 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.420 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.306 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.381 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.440 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.496 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.426 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.391 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.426 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.426 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.537 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.414 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 377 | 386 | PF00179 | 0.309 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.426 |
TRG_DiLeu_BaEn_4 | 256 | 262 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.330 |
TRG_NES_CRM1_1 | 385 | 399 | PF08389 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBS5 | Leptomonas seymouri | 77% | 98% |
A0A0S4KLA7 | Bodo saltans | 33% | 100% |
A0A1X0P5K9 | Trypanosomatidae | 34% | 100% |
A0A3Q8IV97 | Leishmania donovani | 100% | 100% |
A0A3R7L2W7 | Trypanosoma rangeli | 34% | 99% |
A4HMR6 | Leishmania braziliensis | 92% | 100% |
C9ZZB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AF66 | Leishmania major | 97% | 100% |
E9B6C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
O60749 | Homo sapiens | 24% | 80% |
P0C220 | Macaca fascicularis | 23% | 80% |
Q2TBW7 | Bos taurus | 23% | 80% |
Q5R9A9 | Pongo abelii | 23% | 80% |
Q9C0U7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 72% |
Q9CWK8 | Mus musculus | 23% | 80% |
V5B3T2 | Trypanosoma cruzi | 35% | 99% |