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: A4HUT5
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 | 120 | 124 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.258 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.576 |
DEG_APCC_DBOX_1 | 430 | 438 | PF00400 | 0.453 |
DEG_COP1_1 | 505 | 515 | PF00400 | 0.453 |
DEG_ODPH_VHL_1 | 489 | 501 | PF01847 | 0.622 |
DEG_SCF_FBW7_2 | 29 | 35 | PF00400 | 0.501 |
DEG_SPOP_SBC_1 | 138 | 142 | PF00917 | 0.484 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 437 | 443 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 429 | 436 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 385 | 391 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 427 | 433 | PF00149 | 0.527 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.371 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.457 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.736 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 163 | 173 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 277 | 281 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 328 | 338 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 452 | 458 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 64 | 71 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.644 |
LIG_Actin_WH2_2 | 146 | 164 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 386 | 402 | PF00022 | 0.391 |
LIG_AP2alpha_2 | 505 | 507 | PF02296 | 0.522 |
LIG_BIR_III_2 | 7 | 11 | PF00653 | 0.640 |
LIG_BIR_III_4 | 123 | 127 | PF00653 | 0.611 |
LIG_BIR_III_4 | 417 | 421 | PF00653 | 0.560 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.622 |
LIG_CaM_IQ_9 | 295 | 311 | PF13499 | 0.455 |
LIG_Clathr_ClatBox_1 | 266 | 270 | PF01394 | 0.469 |
LIG_Clathr_ClatBox_1 | 501 | 505 | PF01394 | 0.550 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.466 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.630 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.599 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.469 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.383 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.634 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.695 |
LIG_LIR_Gen_1 | 508 | 517 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.530 |
LIG_NRBOX | 243 | 249 | PF00104 | 0.469 |
LIG_PDZ_Class_2 | 513 | 518 | PF00595 | 0.482 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.619 |
LIG_SH2_NCK_1 | 509 | 513 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.436 |
LIG_SH3_1 | 409 | 415 | PF00018 | 0.635 |
LIG_SH3_2 | 92 | 97 | PF14604 | 0.553 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.651 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.635 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.738 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.597 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.633 |
LIG_SUMO_SIM_anti_2 | 496 | 503 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 311 | 316 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 500 | 505 | PF11976 | 0.567 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.510 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.428 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.616 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.629 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.608 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.634 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.250 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.304 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.640 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.568 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.468 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.531 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.383 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.333 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.760 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.691 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.727 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.547 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.484 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.372 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.432 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.570 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.366 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.615 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.745 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.542 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.629 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.576 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.603 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.414 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.328 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.315 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.256 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.312 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.304 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.604 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.591 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.470 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.515 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.413 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.463 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.602 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.723 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.536 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.674 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.325 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.352 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.227 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.587 |
MOD_OFUCOSY | 188 | 195 | PF10250 | 0.270 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.284 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.553 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.626 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.754 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.284 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.613 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.476 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.589 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.248 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.480 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.695 |
MOD_Plk_2-3 | 225 | 231 | PF00069 | 0.303 |
MOD_Plk_2-3 | 376 | 382 | PF00069 | 0.551 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.257 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.618 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.340 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.522 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.369 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.498 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.642 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.444 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.508 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.628 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.248 |
TRG_DiLeu_BaEn_1 | 497 | 502 | PF01217 | 0.600 |
TRG_DiLeu_BaEn_2 | 510 | 516 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF4 | Leptomonas seymouri | 40% | 100% |
A0A3Q8IB69 | Leishmania donovani | 98% | 99% |
A4H9T5 | Leishmania braziliensis | 69% | 100% |
E9ANG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QH57 | Leishmania major | 89% | 100% |