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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 5, no: 6 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0005793 | endoplasmic reticulum-Golgi intermediate compartment | 5 | 1 |
GO:0030134 | COPII-coated ER to Golgi transport vesicle | 8 | 1 |
GO:0030135 | coated vesicle | 7 | 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 |
Related structures:
AlphaFold database: A4H4F2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007029 | endoplasmic reticulum organization | 5 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005537 | mannose binding | 4 | 1 |
GO:0030246 | carbohydrate binding | 2 | 2 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0048029 | monosaccharide binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.363 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.604 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.490 |
DEG_APCC_DBOX_1 | 455 | 463 | PF00400 | 0.343 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.438 |
DOC_CYCLIN_RxL_1 | 213 | 226 | PF00134 | 0.608 |
DOC_MAPK_DCC_7 | 5 | 13 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 360 | 366 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 486 | 492 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 5 | 13 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 102 | 108 | PF00149 | 0.231 |
DOC_PP1_RVXF_1 | 487 | 493 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.244 |
DOC_SPAK_OSR1_1 | 106 | 110 | PF12202 | 0.244 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.253 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.673 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.712 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 310 | 314 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.257 |
LIG_deltaCOP1_diTrp_1 | 166 | 174 | PF00928 | 0.598 |
LIG_deltaCOP1_diTrp_1 | 99 | 107 | PF00928 | 0.338 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.480 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.409 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.546 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.645 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.275 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.275 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.665 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.522 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.417 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.464 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.466 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 45 | 51 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 279 | 288 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.269 |
LIG_PDZ_Class_3 | 500 | 505 | PF00595 | 0.610 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.606 |
LIG_PTB_Apo_2 | 70 | 77 | PF02174 | 0.257 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 135 | 138 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.406 |
LIG_SH3_1 | 494 | 500 | PF00018 | 0.532 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.251 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.604 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 312 | 317 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 348 | 355 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 389 | 395 | PF11976 | 0.485 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.571 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.449 |
LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.400 |
LIG_UBA3_1 | 217 | 223 | PF00899 | 0.608 |
MOD_CDK_SPxxK_3 | 152 | 159 | PF00069 | 0.643 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.195 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.553 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.401 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.530 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.491 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.638 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.511 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.480 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.471 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.412 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.224 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.195 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.363 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.300 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.644 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.500 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.567 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.585 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.478 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.406 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.538 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.369 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.343 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.479 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.624 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.425 |
MOD_PK_1 | 224 | 230 | PF00069 | 0.547 |
MOD_PKA_1 | 223 | 229 | PF00069 | 0.459 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.294 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.279 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.618 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.419 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.481 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.468 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.298 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.432 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.393 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.525 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.298 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.648 |
MOD_Plk_2-3 | 375 | 381 | PF00069 | 0.457 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.454 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.522 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.351 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.468 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.644 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.472 |
MOD_SUMO_for_1 | 372 | 375 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 243 | 248 | PF00179 | 0.280 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.367 |
TRG_NLS_MonoCore_2 | 209 | 214 | PF00514 | 0.593 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.593 |
TRG_NLS_MonoExtN_4 | 207 | 214 | PF00514 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 265 | 270 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA0 | Leptomonas seymouri | 78% | 99% |
A0A1X0NKB0 | Trypanosomatidae | 42% | 78% |
A0A3R7LT82 | Trypanosoma rangeli | 46% | 93% |
A0A3S5H5L7 | Leishmania donovani | 87% | 84% |
A4HSM9 | Leishmania infantum | 87% | 98% |
C9ZU67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 81% |
E8NHN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 83% |
E9AKL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 97% |
Q4QJ95 | Leishmania major | 87% | 100% |
V5ARI9 | Trypanosoma cruzi | 46% | 86% |