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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9ALK6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006399 | tRNA metabolic process | 7 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008033 | tRNA processing | 8 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0034470 | ncRNA processing | 7 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034660 | ncRNA metabolic process | 6 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016432 | tRNA-uridine aminocarboxypropyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.374 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.524 |
CLV_PCSK_FUR_1 | 576 | 580 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.765 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.453 |
CLV_Separin_Metazoa | 224 | 228 | PF03568 | 0.292 |
CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.470 |
DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.392 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.520 |
DEG_COP1_1 | 566 | 574 | PF00400 | 0.415 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 |
DOC_CDC14_PxL_1 | 520 | 528 | PF14671 | 0.341 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.351 |
DOC_MAPK_DCC_7 | 132 | 141 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 168 | 174 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 31 | 37 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 375 | 382 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 132 | 141 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.292 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.351 |
DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.591 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.473 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 585 | 591 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.351 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.292 |
LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.351 |
LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.346 |
LIG_EVH1_1 | 359 | 363 | PF00568 | 0.247 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.488 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.292 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.357 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.683 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.728 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.313 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.357 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.436 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.500 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.480 |
LIG_HP1_1 | 401 | 405 | PF01393 | 0.351 |
LIG_IBAR_NPY_1 | 28 | 30 | PF08397 | 0.430 |
LIG_LIR_Apic_2 | 573 | 577 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.303 |
LIG_PTB_Apo_2 | 472 | 479 | PF02174 | 0.397 |
LIG_PTB_Apo_2 | 524 | 531 | PF02174 | 0.454 |
LIG_PTB_Phospho_1 | 524 | 530 | PF10480 | 0.462 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.509 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.372 |
LIG_SH2_GRB2like | 473 | 476 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.414 |
LIG_SH2_SRC | 473 | 476 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.350 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.508 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.383 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.565 |
LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.326 |
LIG_SxIP_EBH_1 | 556 | 567 | PF03271 | 0.326 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.468 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.307 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.510 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.387 |
LIG_UBA3_1 | 414 | 420 | PF00899 | 0.292 |
LIG_WW_3 | 53 | 57 | PF00397 | 0.471 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.449 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.613 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.747 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.351 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.524 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.442 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.483 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.274 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.285 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.331 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.379 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.502 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.500 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.586 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.356 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.263 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.290 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.502 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.489 |
MOD_GlcNHglycan | 514 | 518 | PF01048 | 0.524 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.459 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.692 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.371 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.521 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.516 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.440 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.464 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.289 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.313 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.529 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.376 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.551 |
MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.413 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.591 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.292 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.236 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.339 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.292 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.495 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.351 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.335 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.274 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.300 |
MOD_PK_1 | 168 | 174 | PF00069 | 0.393 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.388 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.292 |
MOD_PKA_1 | 584 | 590 | PF00069 | 0.480 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.388 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.357 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.292 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.435 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.272 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.513 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.655 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.592 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.399 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.313 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.361 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.292 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.419 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.292 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.313 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.351 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.351 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.404 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.357 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.460 |
MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.351 |
TRG_DiLeu_BaEn_2 | 147 | 153 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.495 |
TRG_NLS_MonoExtC_3 | 418 | 423 | PF00514 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6V5 | Leptomonas seymouri | 55% | 100% |
A0A0S4JPN0 | Bodo saltans | 37% | 100% |
A0A3Q8IHF3 | Leishmania donovani | 87% | 99% |
A4HHL7 | Leishmania braziliensis | 74% | 100% |
A4I4S6 | Leishmania infantum | 87% | 99% |
E9AE79 | Leishmania major | 86% | 100% |