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 |
Related structures:
AlphaFold database: E9ADP6
Term | Name | Level | Count |
---|---|---|---|
GO:0000730 | DNA recombinase assembly | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006312 | mitotic recombination | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0042148 | strand invasion | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065004 | protein-DNA complex assembly | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0090735 | DNA repair complex assembly | 6 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000150 | DNA strand exchange activity | 4 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.269 |
CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.269 |
CLV_PCSK_PC7_1 | 161 | 167 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.560 |
CLV_Separin_Metazoa | 454 | 458 | PF03568 | 0.447 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.526 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.622 |
DEG_APCC_DBOX_1 | 240 | 248 | PF00400 | 0.459 |
DEG_COP1_1 | 432 | 440 | PF00400 | 0.308 |
DEG_MDM2_SWIB_1 | 297 | 305 | PF02201 | 0.469 |
DEG_SPOP_SBC_1 | 581 | 585 | PF00917 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 458 | 464 | PF00134 | 0.541 |
DOC_MAPK_DCC_7 | 594 | 602 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 594 | 602 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.663 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.719 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 21 | 26 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 433 | 438 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 447 | 453 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 472 | 476 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 615 | 625 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 146 | 163 | PF00022 | 0.507 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_EH1_1 | 619 | 627 | PF00400 | 0.516 |
LIG_EVH1_1 | 172 | 176 | PF00568 | 0.665 |
LIG_FAT_LD_1 | 146 | 154 | PF03623 | 0.564 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.547 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.398 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.398 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.484 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.453 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.525 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.650 |
LIG_LIR_Gen_1 | 343 | 351 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 547 | 558 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.530 |
LIG_MYND_1 | 89 | 93 | PF01753 | 0.646 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.469 |
LIG_PCNA_yPIPBox_3 | 313 | 322 | PF02747 | 0.469 |
LIG_PDZ_Class_3 | 645 | 650 | PF00595 | 0.469 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.469 |
LIG_RPA_C_Fungi | 138 | 150 | PF08784 | 0.464 |
LIG_RPA_C_Fungi | 374 | 386 | PF08784 | 0.411 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.304 |
LIG_SH3_1 | 628 | 634 | PF00018 | 0.272 |
LIG_SH3_2 | 52 | 57 | PF14604 | 0.596 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.682 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.500 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.602 |
LIG_SH3_3 | 628 | 634 | PF00018 | 0.304 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.816 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 211 | 216 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 242 | 251 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 506 | 512 | PF11976 | 0.304 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.525 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.521 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.510 |
LIG_WW_3 | 174 | 178 | PF00397 | 0.629 |
MOD_CDK_SPxxK_3 | 358 | 365 | PF00069 | 0.474 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.571 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.643 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.308 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.298 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.242 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.593 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.761 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.451 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.511 |
MOD_DYRK1A_RPxSP_1 | 577 | 581 | PF00069 | 0.369 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.615 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.635 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.497 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.575 |
MOD_GlcNHglycan | 275 | 279 | PF01048 | 0.283 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.304 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.425 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.703 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.329 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.296 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.513 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.366 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.751 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.595 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.304 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.625 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.497 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.317 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.304 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.714 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.583 |
MOD_N-GLC_2 | 549 | 551 | PF02516 | 0.304 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.513 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.605 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.484 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.531 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.304 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.313 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.282 |
MOD_OFUCOSY | 430 | 435 | PF10250 | 0.431 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.521 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.304 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.588 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.523 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.591 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.595 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.470 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.304 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.598 |
MOD_PKB_1 | 577 | 585 | PF00069 | 0.304 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.303 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.433 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.304 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.528 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.481 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.312 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.304 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.680 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.442 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.557 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.317 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.644 |
TRG_DiLeu_BaEn_1 | 454 | 459 | PF01217 | 0.445 |
TRG_DiLeu_BaEn_4 | 197 | 203 | PF01217 | 0.491 |
TRG_DiLeu_LyEn_5 | 454 | 459 | PF01217 | 0.445 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 539 | 542 | PF00400 | 0.313 |
TRG_NES_CRM1_1 | 54 | 67 | PF08389 | 0.472 |
TRG_NLS_MonoExtC_3 | 223 | 228 | PF00514 | 0.507 |
TRG_NLS_MonoExtN_4 | 574 | 580 | PF00514 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U1 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IE59 | Leishmania donovani | 87% | 100% |
A4HH46 | Leishmania braziliensis | 71% | 100% |
A4I499 | Leishmania infantum | 87% | 100% |
E9AM34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |