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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HAE7
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 | 394 | 398 | PF00656 | 0.347 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.419 |
CLV_PCSK_FUR_1 | 564 | 568 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 404 | 407 | PF00134 | 0.489 |
DOC_MAPK_gen_1 | 417 | 423 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 478 | 484 | PF00069 | 0.291 |
DOC_MAPK_RevD_3 | 553 | 567 | PF00069 | 0.385 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.355 |
DOC_PP4_FxxP_1 | 224 | 227 | PF00568 | 0.642 |
DOC_SPAK_OSR1_1 | 121 | 125 | PF12202 | 0.404 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.503 |
DOC_USP7_MATH_2 | 525 | 531 | PF00917 | 0.266 |
DOC_USP7_UBL2_3 | 225 | 229 | PF12436 | 0.706 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.302 |
LIG_14-3-3_CanoR_1 | 209 | 216 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 22 | 29 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 357 | 366 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 436 | 446 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 589 | 594 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 268 | 285 | PF00022 | 0.470 |
LIG_APCC_ABBA_1 | 541 | 546 | PF00400 | 0.291 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.399 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.327 |
LIG_deltaCOP1_diTrp_1 | 307 | 315 | PF00928 | 0.377 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.303 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.486 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.285 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.433 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.708 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.352 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.308 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.532 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.371 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.486 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 316 | 324 | PF00786 | 0.427 |
LIG_GBD_Chelix_1 | 55 | 63 | PF00786 | 0.335 |
LIG_LIR_Apic_2 | 159 | 164 | PF02991 | 0.475 |
LIG_LIR_Apic_2 | 222 | 227 | PF02991 | 0.643 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.518 |
LIG_LIR_Apic_2 | 429 | 435 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 505 | 510 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 537 | 547 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 591 | 600 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 530 | 534 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 548 | 553 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 591 | 596 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.307 |
LIG_LYPXL_S_1 | 99 | 103 | PF13949 | 0.404 |
LIG_LYPXL_yS_3 | 100 | 103 | PF13949 | 0.404 |
LIG_LYPXL_yS_3 | 43 | 46 | PF13949 | 0.284 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.351 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.392 |
LIG_PTB_Phospho_1 | 247 | 253 | PF10480 | 0.396 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.465 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.294 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.404 |
LIG_SH3_1 | 161 | 167 | PF00018 | 0.462 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.517 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.404 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.226 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.671 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.354 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.438 |
LIG_SUMO_SIM_par_1 | 452 | 457 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 551 | 557 | PF11976 | 0.431 |
LIG_TRFH_1 | 403 | 407 | PF08558 | 0.334 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.335 |
LIG_UBA3_1 | 149 | 154 | PF00899 | 0.466 |
LIG_UBA3_1 | 469 | 478 | PF00899 | 0.193 |
MOD_CDC14_SPxK_1 | 226 | 229 | PF00782 | 0.480 |
MOD_CDK_SPK_2 | 223 | 228 | PF00069 | 0.482 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.481 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.290 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.515 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.355 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.726 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.491 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.481 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.528 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.455 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.617 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.266 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.607 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.413 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.605 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.506 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.518 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.661 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.498 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.353 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.355 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.603 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.603 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.593 |
MOD_GlcNHglycan | 362 | 366 | PF01048 | 0.534 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.480 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.445 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.517 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.605 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.770 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.695 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.391 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.556 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.635 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.684 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.675 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.502 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.506 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.649 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.500 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.281 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.259 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.416 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.321 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.325 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.523 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.473 |
MOD_PKA_1 | 228 | 234 | PF00069 | 0.612 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.412 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.516 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.800 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.432 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.582 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.308 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.302 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.456 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.708 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.281 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.314 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.333 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.415 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.269 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.482 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.569 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.680 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.522 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.329 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.519 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.303 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.480 |
MOD_SUMO_for_1 | 523 | 526 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 425 | 435 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_2 | 117 | 123 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 549 | 554 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.193 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 563 | 566 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.193 |
TRG_NES_CRM1_1 | 265 | 279 | PF08389 | 0.239 |
TRG_NLS_Bipartite_1 | 575 | 590 | PF00514 | 0.516 |
TRG_NLS_MonoCore_2 | 585 | 590 | PF00514 | 0.620 |
TRG_NLS_MonoExtN_4 | 583 | 590 | PF00514 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.271 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXU4 | Leptomonas seymouri | 54% | 100% |
A0A1X0P8R7 | Trypanosomatidae | 38% | 100% |
A0A3Q8IH77 | Leishmania donovani | 76% | 100% |
A0A422NFI0 | Trypanosoma rangeli | 37% | 100% |
A4I9K3 | Leishmania infantum | 75% | 100% |
B5APK2 | Leishmania donovani | 76% | 100% |
D0A1W5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B4K1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q38BX0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 38% | 100% |
Q4Q3H5 | Leishmania major | 75% | 100% |
V5BRS6 | Trypanosoma cruzi | 36% | 100% |