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: 0 |
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:0000139 | Golgi membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5F9
Term | Name | Level | Count |
---|---|---|---|
GO:0006901 | vesicle coating | 6 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016050 | vesicle organization | 5 | 2 |
GO:0048200 | Golgi transport vesicle coating | 7 | 2 |
GO:0048205 | COPI coating of Golgi vesicle | 8 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 12 |
GO:0008047 | enzyme activator activity | 3 | 12 |
GO:0030234 | enzyme regulator activity | 2 | 12 |
GO:0030695 | GTPase regulator activity | 4 | 12 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
GO:0140677 | molecular function activator activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.329 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.310 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 65 | 69 | PF00917 | 0.329 |
DOC_ANK_TNKS_1 | 294 | 301 | PF00023 | 0.533 |
DOC_CDC14_PxL_1 | 110 | 118 | PF14671 | 0.498 |
DOC_CKS1_1 | 102 | 107 | PF01111 | 0.364 |
DOC_MAPK_gen_1 | 10 | 18 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 77 | 86 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 90 | 96 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.310 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.379 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.657 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.329 |
LIG_APCC_ABBAyCdc20_2 | 91 | 97 | PF00400 | 0.379 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_4 | 376 | 380 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.325 |
LIG_CaM_NSCaTE_8 | 141 | 148 | PF13499 | 0.558 |
LIG_deltaCOP1_diTrp_1 | 133 | 141 | PF00928 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 393 | 402 | PF00928 | 0.663 |
LIG_deltaCOP1_diTrp_1 | 71 | 76 | PF00928 | 0.294 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.544 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.575 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.762 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.685 |
LIG_LIR_Apic_2 | 133 | 139 | PF02991 | 0.395 |
LIG_LIR_Apic_2 | 344 | 350 | PF02991 | 0.749 |
LIG_LIR_Apic_2 | 5 | 9 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 189 | 195 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.294 |
LIG_PDZ_Class_3 | 397 | 402 | PF00595 | 0.708 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.495 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 6 | 9 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.310 |
LIG_SH3_2 | 102 | 107 | PF14604 | 0.351 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.765 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.283 |
LIG_TYR_ITSM | 284 | 291 | PF00017 | 0.658 |
MOD_CDC14_SPxK_1 | 349 | 352 | PF00782 | 0.748 |
MOD_CDK_SPK_2 | 5 | 10 | PF00069 | 0.334 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.403 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.774 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.372 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.583 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.547 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.750 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.563 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.713 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.724 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.665 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.472 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.772 |
MOD_CMANNOS | 73 | 76 | PF00535 | 0.294 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.469 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.544 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.537 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.536 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.730 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.690 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.536 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.298 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.621 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.497 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.512 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.524 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.695 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.610 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.746 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.745 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.716 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.294 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.415 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.633 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.702 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.324 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.262 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.294 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.564 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.208 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.727 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.691 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.688 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.689 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.329 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.403 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.736 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.705 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.572 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.572 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.647 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.396 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.151 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.367 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.731 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.383 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.611 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.623 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.734 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.559 |
MOD_SUMO_for_1 | 9 | 12 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 71 | 78 | PF00179 | 0.208 |
MOD_SUMO_rev_2 | 97 | 102 | PF00179 | 0.208 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.752 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.750 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMX1 | Leptomonas seymouri | 57% | 100% |
A0A0S4KJM8 | Bodo saltans | 40% | 72% |
A0A1X0NUZ4 | Trypanosomatidae | 50% | 100% |
A0A3Q8IGX3 | Leishmania donovani | 89% | 100% |
A0A422P1B3 | Trypanosoma rangeli | 52% | 100% |
A4HKB0 | Leishmania braziliensis | 71% | 99% |
A4I7U0 | Leishmania infantum | 89% | 100% |
D0AA00 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B2P8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q62848 | Rattus norvegicus | 34% | 97% |
Q8N6T3 | Homo sapiens | 34% | 99% |
Q9EPJ9 | Mus musculus | 35% | 97% |
V5BGP1 | Trypanosoma cruzi | 49% | 100% |