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: A4HMR6
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 | 0.334 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.303 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.290 |
CLV_PCSK_PC7_1 | 106 | 112 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.562 |
DEG_APCC_DBOX_1 | 109 | 117 | PF00400 | 0.300 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.300 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.300 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.560 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 226 | 232 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.314 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 80 | 89 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 389 | 398 | PF00069 | 0.417 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.355 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.285 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 149 | 159 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 335 | 344 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.396 |
LIG_APCC_ABBA_1 | 373 | 378 | PF00400 | 0.394 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.567 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.421 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.344 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.399 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.387 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.421 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 370 | 378 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 405 | 413 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 405 | 409 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.283 |
LIG_Pex14_2 | 246 | 250 | PF04695 | 0.285 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.412 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.417 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.417 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 28 | 31 | PF00017 | 0.468 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.124 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.213 |
LIG_SH3_2 | 144 | 149 | PF14604 | 0.577 |
LIG_SH3_2 | 69 | 74 | PF14604 | 0.285 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.586 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.291 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.386 |
LIG_SUMO_SIM_par_1 | 392 | 397 | PF11976 | 0.417 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.636 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.417 |
LIG_TYR_ITIM | 116 | 121 | PF00017 | 0.417 |
LIG_WW_3 | 146 | 150 | PF00397 | 0.566 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.598 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.518 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.442 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.427 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.407 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.552 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.410 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.417 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.303 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.194 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.417 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.658 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.690 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.578 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.615 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.463 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.417 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.334 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.332 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.459 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.633 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.591 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.543 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.519 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.357 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.392 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.421 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.403 |
MOD_LATS_1 | 236 | 242 | PF00433 | 0.421 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.489 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.503 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.368 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.401 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.464 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.385 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.565 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.421 |
MOD_NEK2_2 | 318 | 323 | PF00069 | 0.288 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.540 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.608 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.461 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.325 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.417 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.300 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.417 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.207 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.285 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.359 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.457 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.417 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.417 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.418 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.417 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.417 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.421 |
MOD_SUMO_for_1 | 402 | 405 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 378 | 387 | PF00179 | 0.297 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_4 | 257 | 263 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.285 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.414 |
TRG_NES_CRM1_1 | 386 | 400 | PF08389 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.374 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBS5 | Leptomonas seymouri | 75% | 98% |
A0A0S4KLA7 | Bodo saltans | 33% | 100% |
A0A1X0P5K9 | Trypanosomatidae | 33% | 100% |
A0A3Q8IV97 | Leishmania donovani | 92% | 100% |
A0A3R7L2W7 | Trypanosoma rangeli | 35% | 99% |
A4IBF2 | Leishmania infantum | 92% | 100% |
C9ZZB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AF66 | Leishmania major | 93% | 100% |
E9B6C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O60749 | Homo sapiens | 22% | 81% |
P0C220 | Macaca fascicularis | 21% | 80% |
Q5R9A9 | Pongo abelii | 21% | 80% |
Q8L5Z7 | Arabidopsis thaliana | 21% | 71% |
Q9C0U7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 73% |
Q9CWK8 | Mus musculus | 22% | 81% |
V5B3T2 | Trypanosoma cruzi | 35% | 99% |