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: A4I499
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 | 43 | 47 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.269 |
CLV_PCSK_FUR_1 | 164 | 168 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.269 |
CLV_PCSK_PC7_1 | 160 | 166 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 453 | 457 | PF03568 | 0.441 |
DEG_APCC_DBOX_1 | 105 | 113 | PF00400 | 0.484 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.597 |
DEG_MDM2_SWIB_1 | 296 | 304 | PF02201 | 0.469 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.496 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.515 |
DOC_CYCLIN_RxL_1 | 607 | 616 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 457 | 463 | PF00134 | 0.530 |
DOC_MAPK_DCC_7 | 593 | 601 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 593 | 601 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.646 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 485 | 495 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 578 | 584 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 614 | 624 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.467 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.629 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 586 | 590 | PF00533 | 0.430 |
LIG_Clathr_ClatBox_1 | 506 | 510 | PF01394 | 0.422 |
LIG_DLG_GKlike_1 | 487 | 495 | PF00625 | 0.292 |
LIG_EH1_1 | 618 | 626 | PF00400 | 0.516 |
LIG_EVH1_1 | 171 | 175 | PF00568 | 0.648 |
LIG_FAT_LD_1 | 145 | 153 | PF03623 | 0.521 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.495 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.401 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.396 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.564 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.484 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.471 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.659 |
LIG_LIR_Apic_2 | 249 | 255 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 546 | 557 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.482 |
LIG_MYND_1 | 88 | 92 | PF01753 | 0.650 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.469 |
LIG_PCNA_yPIPBox_3 | 312 | 321 | PF02747 | 0.469 |
LIG_PDZ_Class_3 | 644 | 649 | PF00595 | 0.469 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.469 |
LIG_RPA_C_Fungi | 373 | 385 | PF08784 | 0.413 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.304 |
LIG_SH3_2 | 51 | 56 | PF14604 | 0.595 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.660 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.550 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.601 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.352 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.800 |
LIG_SUMO_SIM_anti_2 | 111 | 117 | PF11976 | 0.551 |
LIG_SUMO_SIM_anti_2 | 196 | 205 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 241 | 250 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.304 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.486 |
LIG_WW_3 | 173 | 177 | PF00397 | 0.618 |
MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.564 |
MOD_CDK_SPxxK_3 | 357 | 364 | PF00069 | 0.602 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.594 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.565 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.610 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.308 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.295 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.242 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.584 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.777 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.446 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.401 |
MOD_DYRK1A_RPxSP_1 | 576 | 580 | PF00069 | 0.369 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.628 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.676 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.563 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.601 |
MOD_GlcNHglycan | 274 | 278 | PF01048 | 0.382 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.304 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.655 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.506 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.465 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.311 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.294 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.366 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.687 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.536 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.304 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.343 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.586 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.314 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.304 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.681 |
MOD_N-GLC_2 | 548 | 550 | PF02516 | 0.304 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.549 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.550 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.660 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.347 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.304 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.313 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.282 |
MOD_OFUCOSY | 429 | 434 | PF10250 | 0.426 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.304 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.605 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.538 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.460 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.304 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.602 |
MOD_PKB_1 | 485 | 493 | PF00069 | 0.429 |
MOD_PKB_1 | 576 | 584 | PF00069 | 0.304 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.334 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.428 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.304 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.515 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.473 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.451 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.445 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.315 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.674 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.569 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.568 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.317 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.717 |
MOD_SUMO_rev_2 | 220 | 229 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.435 |
TRG_DiLeu_LyEn_5 | 453 | 458 | PF01217 | 0.440 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.313 |
TRG_NLS_MonoExtN_4 | 573 | 579 | PF00514 | 0.313 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U1 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IE59 | Leishmania donovani | 99% | 100% |
A4HH46 | Leishmania braziliensis | 70% | 98% |
E9ADP6 | Leishmania major | 87% | 100% |
E9AM34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |