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: A0A3Q8IB69
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 | 0.590 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.455 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.274 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.516 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.426 |
DEG_COP1_1 | 508 | 518 | PF00400 | 0.468 |
DEG_ODPH_VHL_1 | 492 | 504 | PF01847 | 0.606 |
DEG_SCF_FBW7_2 | 29 | 35 | PF00400 | 0.517 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.466 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 440 | 446 | PF00134 | 0.394 |
DOC_MAPK_gen_1 | 432 | 439 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 388 | 394 | PF00149 | 0.420 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.732 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 165 | 175 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 331 | 341 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 64 | 71 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.681 |
LIG_Actin_WH2_2 | 148 | 166 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 389 | 405 | PF00022 | 0.385 |
LIG_AP2alpha_2 | 508 | 510 | PF02296 | 0.559 |
LIG_BIR_III_2 | 7 | 11 | PF00653 | 0.613 |
LIG_BIR_III_4 | 123 | 127 | PF00653 | 0.585 |
LIG_BIR_III_4 | 420 | 424 | PF00653 | 0.533 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.595 |
LIG_CaM_IQ_9 | 298 | 314 | PF13499 | 0.445 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.459 |
LIG_Clathr_ClatBox_1 | 504 | 508 | PF01394 | 0.582 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.480 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.623 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.599 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.453 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.404 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.614 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.683 |
LIG_LIR_Gen_1 | 511 | 520 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 517 | 521 | PF02991 | 0.545 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.459 |
LIG_PDZ_Class_2 | 516 | 521 | PF00595 | 0.481 |
LIG_Pex14_1 | 356 | 360 | PF04695 | 0.610 |
LIG_SH2_NCK_1 | 512 | 516 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.445 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.605 |
LIG_SH3_2 | 92 | 97 | PF14604 | 0.555 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.625 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.605 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.744 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.611 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.621 |
LIG_SUMO_SIM_anti_2 | 499 | 506 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 268 | 274 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 314 | 319 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 503 | 508 | PF11976 | 0.589 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.491 |
LIG_WRC_WIRS_1 | 515 | 520 | PF05994 | 0.431 |
MOD_CDC14_SPxK_1 | 414 | 417 | PF00782 | 0.589 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.612 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.580 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.621 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.366 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.301 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.612 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.571 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.580 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.524 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.440 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.335 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.772 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.687 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.718 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.539 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.476 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.375 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.417 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.482 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.335 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.605 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.556 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.534 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.629 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.574 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.636 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.415 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.371 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.329 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.245 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.311 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.290 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.582 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.632 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.599 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.511 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.433 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.483 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.605 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.749 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.597 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.668 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.322 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.306 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.289 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.582 |
MOD_OFUCOSY | 190 | 197 | PF10250 | 0.255 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.283 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.504 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.611 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.752 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.321 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.563 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.479 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.659 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.236 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.637 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.683 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.282 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.542 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.244 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.630 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.360 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.590 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.355 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.508 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.628 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.480 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.530 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 228 | 233 | PF01217 | 0.236 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.592 |
TRG_DiLeu_BaEn_2 | 513 | 519 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF4 | Leptomonas seymouri | 40% | 100% |
A4H9T5 | Leishmania braziliensis | 69% | 100% |
A4HUT5 | Leishmania infantum | 98% | 99% |
E9ANG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QH57 | Leishmania major | 90% | 100% |