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:0016020 | membrane | 2 | 12 |
GO:0017119 | Golgi transport complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0099023 | vesicle tethering complex | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000139 | Golgi membrane | 5 | 3 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0098588 | bounding membrane of organelle | 4 | 3 |
Related structures:
AlphaFold database: A4I425
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.366 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.401 |
DEG_SCF_FBW7_1 | 505 | 510 | PF00400 | 0.597 |
DOC_CDC14_PxL_1 | 410 | 418 | PF14671 | 0.570 |
DOC_CKS1_1 | 502 | 507 | PF01111 | 0.599 |
DOC_CYCLIN_RxL_1 | 187 | 199 | PF00134 | 0.443 |
DOC_CYCLIN_RxL_1 | 381 | 391 | PF00134 | 0.506 |
DOC_CYCLIN_yCln2_LP_2 | 437 | 443 | PF00134 | 0.452 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.292 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 318 | 322 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 331 | 335 | PF00244 | 0.452 |
LIG_APCC_ABBAyCdc20_2 | 103 | 109 | PF00400 | 0.308 |
LIG_Clathr_ClatBox_1 | 111 | 115 | PF01394 | 0.308 |
LIG_Clathr_ClatBox_1 | 473 | 477 | PF01394 | 0.505 |
LIG_EH1_1 | 443 | 451 | PF00400 | 0.486 |
LIG_EH1_1 | 466 | 474 | PF00400 | 0.528 |
LIG_eIF4E_1 | 163 | 169 | PF01652 | 0.428 |
LIG_eIF4E_1 | 467 | 473 | PF01652 | 0.407 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.455 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.362 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.538 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.548 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.410 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.606 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.396 |
LIG_GBD_Chelix_1 | 368 | 376 | PF00786 | 0.377 |
LIG_LIR_Gen_1 | 21 | 31 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 378 | 387 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 59 | 67 | PF02991 | 0.455 |
LIG_LIR_LC3C_4 | 272 | 277 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.455 |
LIG_LRP6_Inhibitor_1 | 377 | 383 | PF00058 | 0.299 |
LIG_LYPXL_yS_3 | 439 | 442 | PF13949 | 0.392 |
LIG_MAD2 | 87 | 95 | PF02301 | 0.455 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.347 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.428 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.308 |
LIG_SH2_PTP2 | 211 | 214 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 128 | 131 | PF00017 | 0.416 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 66 | 69 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.416 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.363 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.514 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.673 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.744 |
LIG_SUMO_SIM_anti_2 | 271 | 277 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 87 | 94 | PF11976 | 0.428 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.417 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.568 |
LIG_TYR_ITIM | 203 | 208 | PF00017 | 0.365 |
LIG_TYR_ITIM | 209 | 214 | PF00017 | 0.365 |
LIG_TYR_ITIM | 437 | 442 | PF00017 | 0.452 |
LIG_TYR_ITSM | 159 | 166 | PF00017 | 0.428 |
LIG_UBA3_1 | 208 | 216 | PF00899 | 0.416 |
LIG_UBA3_1 | 297 | 305 | PF00899 | 0.416 |
LIG_WRC_WIRS_1 | 376 | 381 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 427 | 432 | PF05994 | 0.442 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.464 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.398 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.640 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.388 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.631 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.643 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.539 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.258 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.602 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.332 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.362 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.351 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.343 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.649 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.546 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.679 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.728 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.425 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.428 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.439 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.303 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.449 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.673 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.414 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.645 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.384 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.324 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.642 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.642 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.428 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.377 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.460 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.567 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.511 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.532 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.303 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.549 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.568 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.343 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.435 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.406 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.478 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.429 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.369 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.428 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.428 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.645 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.437 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.393 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.435 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.428 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.385 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.535 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.537 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.398 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.556 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.428 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.452 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.560 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.633 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.455 |
TRG_DiLeu_BaEn_1 | 397 | 402 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_1 | 93 | 98 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_2 | 422 | 428 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.443 |
TRG_NES_CRM1_1 | 109 | 122 | PF08389 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 399 | 404 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS6 | Leptomonas seymouri | 72% | 88% |
A0A0S4IRC0 | Bodo saltans | 34% | 100% |
A0A1X0NS75 | Trypanosomatidae | 39% | 100% |
A0A3R7LW05 | Trypanosoma rangeli | 37% | 100% |
A0A3S7X1Y9 | Leishmania donovani | 100% | 100% |
A4HGZ3 | Leishmania braziliensis | 86% | 100% |
D0A8Y2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B0B2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q2TBH9 | Bos taurus | 25% | 85% |
Q4Q7X2 | Leishmania major | 93% | 100% |
Q55BB8 | Dictyostelium discoideum | 20% | 68% |
Q84K25 | Arabidopsis thaliana | 23% | 93% |
Q96MW5 | Homo sapiens | 24% | 86% |
Q9JJA2 | Mus musculus | 24% | 83% |
V5BI51 | Trypanosoma cruzi | 38% | 100% |