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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HHX7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0016197 | endosomal transport | 4 | 7 |
GO:0016482 | cytosolic transport | 4 | 7 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 7 |
GO:0046907 | intracellular transport | 3 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051641 | cellular localization | 2 | 7 |
GO:0051649 | establishment of localization in cell | 3 | 7 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0099022 | vesicle tethering | 4 | 1 |
GO:0099041 | vesicle tethering to Golgi | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.749 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.522 |
DEG_SCF_FBW7_1 | 76 | 81 | PF00400 | 0.450 |
DEG_SPOP_SBC_1 | 363 | 367 | PF00917 | 0.497 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.489 |
DOC_CKS1_1 | 463 | 468 | PF01111 | 0.495 |
DOC_MAPK_MEF2A_6 | 218 | 225 | PF00069 | 0.487 |
DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.630 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.412 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 158 | 165 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 53 | 57 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 82 | 99 | PF00022 | 0.438 |
LIG_APCC_ABBA_1 | 87 | 92 | PF00400 | 0.449 |
LIG_CORNRBOX | 237 | 245 | PF00104 | 0.276 |
LIG_EH1_1 | 239 | 247 | PF00400 | 0.403 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.450 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.389 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.496 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.451 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.473 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.296 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.417 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 133 | 139 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.725 |
LIG_LIR_Gen_1 | 515 | 525 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.316 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.419 |
LIG_Pex14_2 | 518 | 522 | PF04695 | 0.551 |
LIG_RPA_C_Fungi | 499 | 511 | PF08784 | 0.421 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.400 |
LIG_SH2_PTP2 | 156 | 159 | PF00017 | 0.376 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.367 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.538 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.669 |
LIG_SUMO_SIM_anti_2 | 419 | 427 | PF11976 | 0.658 |
LIG_SxIP_EBH_1 | 227 | 238 | PF03271 | 0.486 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.426 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.357 |
LIG_TRFH_1 | 87 | 91 | PF08558 | 0.438 |
LIG_UBA3_1 | 17 | 23 | PF00899 | 0.516 |
MOD_CDK_SPK_2 | 480 | 485 | PF00069 | 0.478 |
MOD_CDK_SPxK_1 | 462 | 468 | PF00069 | 0.492 |
MOD_CDK_SPxxK_3 | 462 | 469 | PF00069 | 0.494 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.451 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.390 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.597 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.678 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.671 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.745 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.330 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.297 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.412 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.635 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.774 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.563 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.562 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.592 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.690 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.642 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.680 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.730 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.731 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.631 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.700 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.565 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.316 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.502 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.409 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.509 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.540 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.614 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.600 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.511 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.586 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.369 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.518 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.477 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.562 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.569 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.473 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.549 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.324 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.638 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.239 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.468 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.537 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.374 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.740 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.654 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.567 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.731 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.334 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.730 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.490 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.439 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.533 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.664 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.651 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.715 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.521 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.630 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.261 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 132 | 139 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_1 | 421 | 426 | PF01217 | 0.717 |
TRG_DiLeu_BaEn_4 | 202 | 208 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P274 | Trypanosomatidae | 31% | 71% |
A0A3R7MQU5 | Trypanosoma rangeli | 34% | 76% |
C9ZQI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 77% |
Q4Q7S6 | Leishmania major | 74% | 100% |
V5DD41 | Trypanosoma cruzi | 34% | 78% |