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. | yes | yes: 15 |
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: 16 |
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 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0030117 | membrane coat | 3 | 12 |
GO:0030120 | vesicle coat | 4 | 12 |
GO:0030126 | COPI vesicle coat | 5 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098588 | bounding membrane of organelle | 4 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005794 | Golgi apparatus | 5 | 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 |
Related structures:
AlphaFold database: A4H8P5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 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:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051645 | Golgi localization | 3 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.320 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.403 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.684 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.173 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.459 |
DEG_SPOP_SBC_1 | 405 | 409 | PF00917 | 0.353 |
DOC_CYCLIN_RxL_1 | 355 | 366 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 488 | 494 | PF00134 | 0.486 |
DOC_MAPK_MEF2A_6 | 284 | 292 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.313 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.440 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.433 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 526 | 534 | PF00244 | 0.417 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.313 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.388 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.378 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.265 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.329 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.349 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.429 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.298 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.355 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.408 |
LIG_LIR_Apic_2 | 217 | 223 | PF02991 | 0.738 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 445 | 456 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 64 | 71 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.383 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.367 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.582 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.440 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.378 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.580 |
LIG_SH2_STAT3 | 58 | 61 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.446 |
LIG_SH3_2 | 423 | 428 | PF14604 | 0.440 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.674 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.313 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.380 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.411 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.339 |
LIG_SUMO_SIM_anti_2 | 326 | 331 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 459 | 464 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 326 | 333 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 458 | 464 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.353 |
LIG_TRAF2_1 | 141 | 144 | PF00917 | 0.434 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.436 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.440 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.445 |
LIG_UBA3_1 | 66 | 75 | PF00899 | 0.355 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.674 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.378 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.340 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.305 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.370 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.256 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.405 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.427 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.440 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.392 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.570 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.537 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.665 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.646 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.640 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.310 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.350 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.414 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.693 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.386 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.356 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.249 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.450 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.403 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.343 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.418 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.440 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.378 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.639 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.682 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.671 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.715 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.443 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.349 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.796 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.417 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.451 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.352 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.603 |
MOD_PKA_1 | 172 | 178 | PF00069 | 0.687 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.462 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.459 |
MOD_PKB_1 | 170 | 178 | PF00069 | 0.590 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.396 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.434 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.596 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.389 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.400 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.238 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.304 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.414 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.527 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.216 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.244 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.514 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.420 |
MOD_Plk_2-3 | 317 | 323 | PF00069 | 0.327 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.315 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.378 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.343 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.439 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.357 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.342 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.366 |
TRG_DiLeu_BaEn_4 | 143 | 149 | PF01217 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.361 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.390 |
TRG_NES_CRM1_1 | 254 | 269 | PF08389 | 0.716 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I039 | Leptomonas seymouri | 75% | 100% |
A0A0S4KK09 | Bodo saltans | 44% | 100% |
A0A1X0NYY5 | Trypanosomatidae | 50% | 97% |
A0A3Q8IAE4 | Leishmania donovani | 87% | 100% |
A0A422N6V7 | Trypanosoma rangeli | 49% | 100% |
A4HX15 | Leishmania infantum | 87% | 100% |
C9ZVY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AQS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P43621 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 98% |
P48444 | Homo sapiens | 31% | 100% |
P49661 | Oryza sativa subsp. japonica | 33% | 100% |
P53619 | Bos taurus | 31% | 100% |
Q09236 | Caenorhabditis elegans | 32% | 100% |
Q0DJ99 | Oryza sativa subsp. japonica | 33% | 100% |
Q0DJA0 | Oryza sativa subsp. japonica | 32% | 100% |
Q4QEP9 | Leishmania major | 86% | 100% |
Q55EZ6 | Dictyostelium discoideum | 30% | 99% |
Q5RA77 | Pongo abelii | 31% | 100% |
Q5XJY5 | Mus musculus | 31% | 100% |
Q5ZL57 | Gallus gallus | 30% | 100% |
Q66H80 | Rattus norvegicus | 31% | 100% |
Q93Y22 | Arabidopsis thaliana | 31% | 100% |
V5BI39 | Trypanosoma cruzi | 50% | 99% |