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: E9ANG9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 6 |
GO:0006974 | DNA damage response | 4 | 6 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
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:0050896 | response to stimulus | 1 | 6 |
GO:0051716 | cellular response to stimulus | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000730 | DNA recombinase assembly | 7 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006312 | mitotic recombination | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0042148 | strand invasion | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065004 | protein-DNA complex assembly | 6 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090735 | DNA repair complex assembly | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
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 |
GO:0000150 | DNA strand exchange activity | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.633 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.592 |
DEG_COP1_1 | 507 | 517 | PF00400 | 0.612 |
DEG_ODPH_VHL_1 | 491 | 503 | PF01847 | 0.783 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.563 |
DOC_CKS1_1 | 414 | 419 | PF01111 | 0.512 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 439 | 445 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 431 | 438 | PF00069 | 0.609 |
DOC_PP1_RVXF_1 | 387 | 393 | PF00149 | 0.566 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.439 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.817 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 164 | 174 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 50 | 60 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.776 |
LIG_Actin_WH2_2 | 147 | 165 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 388 | 404 | PF00022 | 0.516 |
LIG_AP2alpha_2 | 507 | 509 | PF02296 | 0.744 |
LIG_BIR_III_4 | 122 | 126 | PF00653 | 0.734 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.438 |
LIG_CaM_IQ_9 | 297 | 313 | PF13499 | 0.530 |
LIG_Clathr_ClatBox_1 | 268 | 272 | PF01394 | 0.546 |
LIG_Clathr_ClatBox_1 | 503 | 507 | PF01394 | 0.765 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.511 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.737 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.729 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.789 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.854 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.539 |
LIG_Integrin_RGD_1 | 376 | 378 | PF01839 | 0.496 |
LIG_LIR_Gen_1 | 510 | 519 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 510 | 514 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 516 | 520 | PF02991 | 0.637 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.546 |
LIG_PDZ_Class_2 | 515 | 520 | PF00595 | 0.661 |
LIG_Pex14_1 | 355 | 359 | PF04695 | 0.721 |
LIG_SH2_NCK_1 | 511 | 515 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.581 |
LIG_SH3_1 | 109 | 115 | PF00018 | 0.608 |
LIG_SH3_1 | 411 | 417 | PF00018 | 0.717 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.528 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.801 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.717 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.574 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.780 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.712 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.649 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.813 |
LIG_SUMO_SIM_par_1 | 267 | 273 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 313 | 318 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 502 | 507 | PF11976 | 0.771 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.617 |
LIG_WRC_WIRS_1 | 514 | 519 | PF05994 | 0.567 |
MOD_CDC14_SPxK_1 | 93 | 96 | PF00782 | 0.736 |
MOD_CDK_SPxK_1 | 90 | 96 | PF00069 | 0.745 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.699 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.412 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.787 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.697 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.654 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.797 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.856 |
MOD_DYRK1A_RPxSP_1 | 454 | 458 | PF00069 | 0.516 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.811 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.580 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.465 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.497 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.612 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.509 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.786 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.724 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.541 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.752 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.720 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.488 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.433 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.295 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.418 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.419 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.411 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.722 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.561 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.601 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.706 |
MOD_LATS_1 | 124 | 130 | PF00433 | 0.604 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.738 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.781 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.436 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.452 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.302 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.700 |
MOD_OFUCOSY | 189 | 196 | PF10250 | 0.338 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.389 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.787 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.653 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.799 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.389 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.591 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.705 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.605 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.854 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.672 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.452 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.644 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.513 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.714 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.567 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.500 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.649 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.740 |
MOD_SUMO_for_1 | 10 | 13 | PF00179 | 0.735 |
MOD_SUMO_rev_2 | 71 | 81 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_2 | 512 | 518 | PF01217 | 0.553 |
TRG_DiLeu_LyEn_5 | 499 | 504 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF4 | Leptomonas seymouri | 40% | 100% |
A0A3Q8IB69 | Leishmania donovani | 90% | 100% |
A4H9T5 | Leishmania braziliensis | 69% | 100% |
A4HUT5 | Leishmania infantum | 89% | 100% |
Q4QH57 | Leishmania major | 88% | 100% |