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: Q4QH57
Term | Name | Level | Count |
---|---|---|---|
GO:0000730 | DNA recombinase assembly | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006312 | mitotic recombination | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0042148 | strand invasion | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065004 | protein-DNA complex assembly | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
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 | 7 |
GO:0090735 | DNA repair complex assembly | 6 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0006281 | DNA repair | 5 | 5 |
GO:0006950 | response to stress | 2 | 5 |
GO:0006974 | DNA damage response | 4 | 5 |
GO:0033554 | cellular response to stress | 3 | 5 |
GO:0050896 | response to stimulus | 1 | 5 |
GO:0051716 | cellular response to stimulus | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000150 | DNA strand exchange activity | 4 | 2 |
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140299 | small molecule sensor activity | 1 | 7 |
GO:0140612 | DNA damage sensor activity | 2 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.662 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.601 |
DEG_COP1_1 | 508 | 518 | PF00400 | 0.633 |
DEG_ODPH_VHL_1 | 492 | 504 | PF01847 | 0.787 |
DEG_SCF_FBW7_2 | 30 | 35 | PF00400 | 0.638 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.563 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.648 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.537 |
DOC_CYCLIN_yCln2_LP_2 | 440 | 446 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 432 | 439 | PF00069 | 0.619 |
DOC_MAPK_MEF2A_6 | 468 | 476 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 388 | 394 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.644 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.697 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 165 | 175 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 331 | 341 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.710 |
LIG_Actin_WH2_2 | 148 | 166 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 389 | 405 | PF00022 | 0.501 |
LIG_AP2alpha_2 | 508 | 510 | PF02296 | 0.746 |
LIG_BIR_III_2 | 7 | 11 | PF00653 | 0.753 |
LIG_BIR_III_4 | 123 | 127 | PF00653 | 0.739 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.710 |
LIG_CaM_IQ_9 | 298 | 314 | PF13499 | 0.530 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.543 |
LIG_Clathr_ClatBox_1 | 504 | 508 | PF01394 | 0.765 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.543 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.714 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.697 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.536 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.383 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.793 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.849 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.469 |
LIG_LIR_Gen_1 | 511 | 520 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 517 | 521 | PF02991 | 0.671 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.546 |
LIG_PDZ_Class_2 | 516 | 521 | PF00595 | 0.694 |
LIG_SH2_NCK_1 | 512 | 516 | PF00017 | 0.640 |
LIG_SH2_SRC | 342 | 345 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.656 |
LIG_SH3_1 | 110 | 116 | PF00018 | 0.597 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.737 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.495 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.793 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.737 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.572 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.720 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.798 |
LIG_SUMO_SIM_anti_2 | 499 | 506 | PF11976 | 0.747 |
LIG_SUMO_SIM_par_1 | 268 | 274 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 314 | 319 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 503 | 508 | PF11976 | 0.770 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.617 |
LIG_WRC_WIRS_1 | 515 | 520 | PF05994 | 0.613 |
MOD_CDC14_SPxK_1 | 414 | 417 | PF00782 | 0.700 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.722 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.734 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.496 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.412 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.729 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.679 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.498 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.635 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.542 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.635 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.446 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.437 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.790 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.848 |
MOD_DYRK1A_RPxSP_1 | 455 | 459 | PF00069 | 0.510 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.816 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.280 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.465 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.497 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.509 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.683 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.654 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.773 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.648 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.679 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.726 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.717 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.488 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.433 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.418 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.353 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.419 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.411 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.721 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.624 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.513 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.616 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.586 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.580 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.686 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.693 |
MOD_LATS_1 | 125 | 131 | PF00433 | 0.603 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.770 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.659 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.786 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.334 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.430 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.510 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.411 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.695 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.352 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.653 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.790 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.794 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.389 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.675 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.616 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.849 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.397 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.646 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.738 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.493 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.626 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.513 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.563 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.736 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.553 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.493 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.525 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.627 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.724 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.749 |
TRG_DiLeu_BaEn_2 | 513 | 519 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.647 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF4 | Leptomonas seymouri | 39% | 100% |
A0A3Q8IB69 | Leishmania donovani | 90% | 100% |
A4H9T5 | Leishmania braziliensis | 68% | 91% |
A4HUT5 | Leishmania infantum | 89% | 100% |
E9ANG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |