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: A4HH46
Term | Name | Level | Count |
---|---|---|---|
GO:0000730 | DNA recombinase assembly | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006312 | mitotic recombination | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0042148 | strand invasion | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065004 | protein-DNA complex assembly | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090735 | DNA repair complex assembly | 6 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000150 | DNA strand exchange activity | 4 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.269 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.316 |
CLV_Separin_Metazoa | 438 | 442 | PF03568 | 0.443 |
DEG_APCC_DBOX_1 | 161 | 169 | PF00400 | 0.592 |
DEG_MDM2_SWIB_1 | 281 | 289 | PF02201 | 0.469 |
DEG_SPOP_SBC_1 | 471 | 475 | PF00917 | 0.495 |
DEG_SPOP_SBC_1 | 571 | 575 | PF00917 | 0.450 |
DOC_CYCLIN_RxL_1 | 592 | 601 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.533 |
DOC_MAPK_DCC_7 | 578 | 586 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 578 | 586 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 454 | 460 | PF00149 | 0.507 |
DOC_PP2B_LxvP_1 | 166 | 169 | PF13499 | 0.649 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.593 |
DOC_PP4_MxPP_1 | 168 | 171 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 431 | 437 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 472 | 477 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 52 | 59 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 599 | 609 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 140 | 157 | PF00022 | 0.453 |
LIG_BIR_III_2 | 259 | 263 | PF00653 | 0.341 |
LIG_BIR_III_4 | 9 | 13 | PF00653 | 0.497 |
LIG_DLG_GKlike_1 | 472 | 480 | PF00625 | 0.434 |
LIG_EH1_1 | 603 | 611 | PF00400 | 0.516 |
LIG_EVH1_1 | 166 | 170 | PF00568 | 0.650 |
LIG_FAT_LD_1 | 140 | 148 | PF03623 | 0.514 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.414 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.555 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.408 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.360 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.394 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.515 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.412 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.453 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.509 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.678 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.473 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.523 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 244 | 250 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 409 | 416 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 531 | 542 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.500 |
LIG_MYND_1 | 70 | 74 | PF01753 | 0.539 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.469 |
LIG_PCNA_yPIPBox_3 | 297 | 306 | PF02747 | 0.469 |
LIG_PDZ_Class_3 | 629 | 634 | PF00595 | 0.469 |
LIG_Pex14_2 | 281 | 285 | PF04695 | 0.469 |
LIG_RPA_C_Fungi | 358 | 370 | PF08784 | 0.414 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.304 |
LIG_SH3_1 | 612 | 618 | PF00018 | 0.272 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.519 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.662 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.352 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 192 | 200 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 236 | 246 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 53 | 61 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 490 | 496 | PF11976 | 0.304 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 223 | 230 | PF00069 | 0.603 |
MOD_CDK_SPxxK_3 | 342 | 349 | PF00069 | 0.628 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.582 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.535 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.504 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.297 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.629 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.308 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.298 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.242 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.608 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.516 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.786 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.458 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.290 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.451 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.464 |
MOD_DYRK1A_RPxSP_1 | 561 | 565 | PF00069 | 0.369 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.557 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.648 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.521 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.304 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.481 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.314 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.294 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.366 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.554 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.682 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.529 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.624 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.469 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.593 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.304 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.335 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.579 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.625 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.497 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.314 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.304 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.509 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.671 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.579 |
MOD_N-GLC_2 | 533 | 535 | PF02516 | 0.304 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.472 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.603 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.696 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.545 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.527 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.304 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.394 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.313 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.282 |
MOD_NEK2_2 | 116 | 121 | PF00069 | 0.473 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.496 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.507 |
MOD_OFUCOSY | 414 | 419 | PF10250 | 0.426 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.304 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.227 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.595 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.590 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.581 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.463 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.390 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.304 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.398 |
MOD_PKB_1 | 561 | 569 | PF00069 | 0.304 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.304 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.516 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.386 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.401 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.524 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.456 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.515 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.447 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.315 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.668 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.532 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.419 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.605 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.454 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.597 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.591 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.317 |
TRG_DiLeu_BaEn_1 | 438 | 443 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.301 |
TRG_DiLeu_LyEn_5 | 438 | 443 | PF01217 | 0.443 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.568 |
TRG_NLS_MonoExtN_4 | 558 | 564 | PF00514 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.227 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U1 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IE59 | Leishmania donovani | 71% | 98% |
A4I499 | Leishmania infantum | 70% | 98% |
E9ADP6 | Leishmania major | 71% | 100% |
E9AM34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 98% |