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:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q3H5
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008612 | peptidyl-lysine modification to peptidyl-hypusine | 3 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0018193 | peptidyl-amino acid modification | 5 | 11 |
GO:0018205 | peptidyl-lysine modification | 6 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0051604 | protein maturation | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 5 |
GO:0034038 | deoxyhypusine synthase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.340 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 152 | 156 | PF00082 | 0.363 |
CLV_PCSK_FUR_1 | 566 | 570 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.600 |
CLV_Separin_Metazoa | 170 | 174 | PF03568 | 0.424 |
DEG_SPOP_SBC_1 | 440 | 444 | PF00917 | 0.605 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 406 | 412 | PF00134 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 85 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 480 | 486 | PF00069 | 0.291 |
DOC_MAPK_RevD_3 | 555 | 569 | PF00069 | 0.391 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.468 |
DOC_SPAK_OSR1_1 | 121 | 125 | PF12202 | 0.466 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.602 |
DOC_USP7_MATH_2 | 527 | 533 | PF00917 | 0.266 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.619 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 193 | 203 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 437 | 445 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 577 | 587 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 269 | 286 | PF00022 | 0.474 |
LIG_Actin_WH2_2 | 311 | 328 | PF00022 | 0.237 |
LIG_APCC_ABBA_1 | 543 | 548 | PF00400 | 0.284 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.406 |
LIG_BIR_III_2 | 573 | 577 | PF00653 | 0.526 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.323 |
LIG_deltaCOP1_diTrp_1 | 308 | 316 | PF00928 | 0.421 |
LIG_DLG_GKlike_1 | 173 | 181 | PF00625 | 0.453 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.509 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.574 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.420 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.492 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.338 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.308 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.374 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.545 |
LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.429 |
LIG_GBD_Chelix_1 | 457 | 465 | PF00786 | 0.378 |
LIG_GBD_Chelix_1 | 55 | 63 | PF00786 | 0.410 |
LIG_HCF-1_HBM_1 | 97 | 100 | PF13415 | 0.510 |
LIG_LIR_Apic_2 | 159 | 164 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 402 | 407 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 262 | 273 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 42 | 50 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 507 | 512 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.405 |
LIG_LYPXL_S_1 | 99 | 103 | PF13949 | 0.479 |
LIG_LYPXL_yS_3 | 100 | 103 | PF13949 | 0.476 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.348 |
LIG_PTB_Apo_2 | 248 | 255 | PF02174 | 0.381 |
LIG_PTB_Phospho_1 | 248 | 254 | PF10480 | 0.383 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.494 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.512 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.568 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.580 |
LIG_SH3_1 | 161 | 167 | PF00018 | 0.492 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.553 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.424 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.399 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.356 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.560 |
LIG_SUMO_SIM_par_1 | 553 | 559 | PF11976 | 0.399 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.454 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.516 |
LIG_UBA3_1 | 149 | 154 | PF00899 | 0.484 |
LIG_WRC_WIRS_1 | 269 | 274 | PF05994 | 0.326 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.486 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.724 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.517 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.573 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.414 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.533 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.652 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.266 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.661 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.381 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.607 |
MOD_DYRK1A_RPxSP_1 | 230 | 234 | PF00069 | 0.498 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.259 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.471 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.690 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.620 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.308 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.375 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.427 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.741 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.483 |
MOD_GlcNHglycan | 425 | 429 | PF01048 | 0.522 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.645 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.469 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.648 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.675 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.666 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.538 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.372 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.630 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.564 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.660 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.475 |
MOD_LATS_1 | 417 | 423 | PF00433 | 0.610 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.434 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.328 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.302 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.438 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.378 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.429 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.446 |
MOD_PK_1 | 419 | 425 | PF00069 | 0.608 |
MOD_PKA_1 | 438 | 444 | PF00069 | 0.588 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.450 |
MOD_PKA_1 | 578 | 584 | PF00069 | 0.591 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.418 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.450 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.588 |
MOD_PKB_1 | 436 | 444 | PF00069 | 0.590 |
MOD_PKB_1 | 566 | 574 | PF00069 | 0.432 |
MOD_PKB_1 | 577 | 585 | PF00069 | 0.514 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.361 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.308 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.273 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.469 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.318 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.371 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.476 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.317 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.575 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.522 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.547 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.330 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.301 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.473 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.600 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.491 |
MOD_SUMO_for_1 | 525 | 528 | PF00179 | 0.399 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_2 | 117 | 123 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 565 | 568 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.739 |
TRG_NLS_Bipartite_1 | 418 | 439 | PF00514 | 0.586 |
TRG_NLS_MonoCore_2 | 434 | 439 | PF00514 | 0.530 |
TRG_NLS_MonoExtC_3 | 434 | 439 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 432 | 439 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXU4 | Leptomonas seymouri | 55% | 100% |
A0A1X0P8R7 | Trypanosomatidae | 37% | 100% |
A0A3Q8IH77 | Leishmania donovani | 93% | 100% |
A0A422NFI0 | Trypanosoma rangeli | 37% | 100% |
A4HAE7 | Leishmania braziliensis | 75% | 100% |
A4I9K3 | Leishmania infantum | 93% | 100% |
B5APK2 | Leishmania donovani | 93% | 100% |
D0A1W5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B4K1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q38BX0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 38% | 100% |
V5BRS6 | Trypanosoma cruzi | 37% | 100% |