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: E9AM34
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_NRD_NRD_1 | 105 | 107 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.277 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.277 |
CLV_PCSK_PC7_1 | 160 | 166 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.657 |
CLV_Separin_Metazoa | 453 | 457 | PF03568 | 0.465 |
CLV_Separin_Metazoa | 53 | 57 | PF03568 | 0.461 |
DEG_MDM2_SWIB_1 | 296 | 304 | PF02201 | 0.477 |
DEG_SPOP_SBC_1 | 580 | 584 | PF00917 | 0.480 |
DOC_CDC14_PxL_1 | 458 | 466 | PF14671 | 0.413 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 457 | 463 | PF00134 | 0.554 |
DOC_MAPK_DCC_7 | 456 | 466 | PF00069 | 0.391 |
DOC_MAPK_DCC_7 | 593 | 601 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 105 | 112 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 138 | 145 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 432 | 440 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 593 | 601 | PF00069 | 0.480 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.714 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 485 | 492 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 614 | 624 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.532 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.514 |
LIG_EH1_1 | 618 | 626 | PF00400 | 0.535 |
LIG_EVH1_1 | 171 | 175 | PF00568 | 0.717 |
LIG_FAT_LD_1 | 145 | 153 | PF03623 | 0.617 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.444 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.408 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.600 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.499 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.710 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.531 |
LIG_MYND_1 | 88 | 92 | PF01753 | 0.645 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.477 |
LIG_PCNA_yPIPBox_3 | 312 | 321 | PF02747 | 0.477 |
LIG_PDZ_Class_3 | 644 | 649 | PF00595 | 0.477 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.477 |
LIG_RPA_C_Fungi | 373 | 385 | PF08784 | 0.442 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.315 |
LIG_SH3_1 | 627 | 633 | PF00018 | 0.282 |
LIG_SH3_2 | 51 | 56 | PF14604 | 0.606 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.733 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.558 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.617 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.315 |
LIG_Sin3_3 | 334 | 341 | PF02671 | 0.272 |
LIG_SUMO_SIM_anti_2 | 111 | 119 | PF11976 | 0.623 |
LIG_SUMO_SIM_anti_2 | 241 | 248 | PF11976 | 0.529 |
LIG_SUMO_SIM_anti_2 | 435 | 441 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 107 | 114 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.315 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.570 |
LIG_WW_3 | 173 | 177 | PF00397 | 0.672 |
MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.587 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.606 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.581 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.337 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.292 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.251 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.803 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.518 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.208 |
MOD_DYRK1A_RPxSP_1 | 576 | 580 | PF00069 | 0.395 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.639 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.651 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.517 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.693 |
MOD_GlcNHglycan | 274 | 278 | PF01048 | 0.480 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.315 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.309 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.565 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.322 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.418 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.537 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.717 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.682 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.722 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.325 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.315 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.348 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.430 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.315 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.655 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.611 |
MOD_N-GLC_2 | 548 | 550 | PF02516 | 0.315 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.518 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.709 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.532 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.501 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.337 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.328 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.292 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.208 |
MOD_OFUCOSY | 429 | 434 | PF10250 | 0.448 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.315 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.494 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.625 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.556 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.315 |
MOD_PKB_1 | 576 | 584 | PF00069 | 0.315 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.441 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.441 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.315 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.520 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.526 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.567 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.257 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.315 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.673 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.589 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.580 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.559 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.372 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.738 |
MOD_SUMO_rev_2 | 178 | 187 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 220 | 229 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_1 | 493 | 498 | PF01217 | 0.350 |
TRG_DiLeu_LyEn_5 | 453 | 458 | PF01217 | 0.463 |
TRG_DiLeu_LyEn_5 | 493 | 498 | PF01217 | 0.350 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.340 |
TRG_NLS_MonoExtN_4 | 573 | 579 | PF00514 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U1 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IE59 | Leishmania donovani | 86% | 100% |
A4HH46 | Leishmania braziliensis | 69% | 98% |
A4I499 | Leishmania infantum | 86% | 100% |
E9ADP6 | Leishmania major | 83% | 100% |