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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0032045 | guanyl-nucleotide exchange factor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034066 | Ric1-Rgp1 guanyl-nucleotide exchange factor complex | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4IAH0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0016482 | cytosolic transport | 4 | 1 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.497 |
CLV_MEL_PAP_1 | 22 | 28 | PF00089 | 0.459 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.631 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.540 |
DEG_APCC_DBOX_1 | 277 | 285 | PF00400 | 0.578 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.616 |
DEG_ODPH_VHL_1 | 452 | 464 | PF01847 | 0.474 |
DEG_SIAH_1 | 453 | 461 | PF03145 | 0.481 |
DOC_ANK_TNKS_1 | 438 | 445 | PF00023 | 0.588 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.699 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.537 |
DOC_MAPK_DCC_7 | 190 | 198 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 190 | 198 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 69 | 77 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 190 | 198 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 278 | 285 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 69 | 77 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 87 | 94 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.349 |
DOC_PP4_FxxP_1 | 145 | 148 | PF00568 | 0.390 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.515 |
DOC_PP4_FxxP_1 | 403 | 406 | PF00568 | 0.446 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.616 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 176 | 186 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.483 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.713 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.483 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.555 |
LIG_Clathr_ClatBox_1 | 80 | 84 | PF01394 | 0.492 |
LIG_EVH1_1 | 213 | 217 | PF00568 | 0.528 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.532 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.492 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.498 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.377 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.482 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.588 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.721 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.476 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 142 | 148 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 211 | 216 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.429 |
LIG_MYND_1 | 450 | 454 | PF01753 | 0.583 |
LIG_PCNA_PIPBox_1 | 206 | 215 | PF02747 | 0.522 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.579 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.615 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.615 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.464 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.474 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.572 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.673 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.560 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.390 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 311 | 317 | PF11976 | 0.574 |
LIG_SUMO_SIM_anti_2 | 347 | 352 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 74 | 79 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 340 | 345 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 346 | 352 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 71 | 76 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 79 | 86 | PF11976 | 0.436 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.509 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.494 |
LIG_TRFH_1 | 213 | 217 | PF08558 | 0.528 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.439 |
MOD_CDK_SPK_2 | 102 | 107 | PF00069 | 0.529 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.707 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.597 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.586 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.395 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.730 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.626 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.547 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.683 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.646 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.654 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.514 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.589 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.445 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.601 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.581 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.733 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.595 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.484 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.573 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.478 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.543 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.651 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.585 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.571 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.372 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.504 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.305 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.736 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.519 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.514 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.701 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.555 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.412 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.406 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.513 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.418 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.548 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.513 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.525 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.742 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.573 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.567 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.514 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.679 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.496 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.550 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.577 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.432 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.550 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.487 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.502 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.519 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.482 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.533 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.483 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.514 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.450 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.435 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.512 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.534 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.540 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.600 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.514 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.529 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 457 | 462 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.662 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 71 | 76 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I798 | Leptomonas seymouri | 58% | 100% |
A0A1X0PA91 | Trypanosomatidae | 24% | 100% |
A0A3Q8ILJ7 | Leishmania donovani | 100% | 100% |
A0A422NVD8 | Trypanosoma rangeli | 25% | 100% |
A4HBC2 | Leishmania braziliensis | 76% | 100% |
C9ZLS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9B5J4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q2E2 | Leishmania major | 93% | 100% |
V5BRG2 | Trypanosoma cruzi | 25% | 100% |