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: A4H9T5
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 | 476 | 480 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.689 |
CLV_MEL_PAP_1 | 126 | 132 | PF00089 | 0.535 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.705 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 483 | 491 | PF00400 | 0.600 |
DEG_ODPH_VHL_1 | 542 | 554 | PF01847 | 0.764 |
DEG_SCF_FBW7_2 | 94 | 100 | PF00400 | 0.583 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.587 |
DOC_CYCLIN_yCln2_LP_2 | 490 | 496 | PF00134 | 0.472 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.623 |
DOC_PP1_RVXF_1 | 438 | 444 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 480 | 486 | PF00149 | 0.653 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.555 |
DOC_PP4_FxxP_1 | 379 | 382 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 129 | 136 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 215 | 225 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.581 |
LIG_Actin_WH2_2 | 198 | 216 | PF00022 | 0.546 |
LIG_Actin_WH2_2 | 2 | 19 | PF00022 | 0.532 |
LIG_Actin_WH2_2 | 439 | 455 | PF00022 | 0.501 |
LIG_AP2alpha_2 | 558 | 560 | PF02296 | 0.689 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.487 |
LIG_BIR_III_2 | 72 | 76 | PF00653 | 0.751 |
LIG_BIR_III_4 | 52 | 56 | PF00653 | 0.612 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.612 |
LIG_Clathr_ClatBox_1 | 319 | 323 | PF01394 | 0.543 |
LIG_Clathr_ClatBox_1 | 554 | 558 | PF01394 | 0.708 |
LIG_deltaCOP1_diTrp_1 | 558 | 567 | PF00928 | 0.412 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.524 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.550 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.539 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.782 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.776 |
LIG_GSK3_LRP6_1 | 373 | 378 | PF00069 | 0.515 |
LIG_LIR_Apic_2 | 376 | 382 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 156 | 163 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 342 | 351 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 561 | 569 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 342 | 347 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 561 | 565 | PF02991 | 0.609 |
LIG_NRBOX | 296 | 302 | PF00104 | 0.546 |
LIG_OCRL_FandH_1 | 5 | 17 | PF00620 | 0.522 |
LIG_PDZ_Class_2 | 566 | 571 | PF00595 | 0.642 |
LIG_Pex14_1 | 406 | 410 | PF04695 | 0.717 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.521 |
LIG_SH2_NCK_1 | 562 | 566 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.550 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.557 |
LIG_SH3_1 | 122 | 128 | PF00018 | 0.484 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.539 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.476 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.790 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.683 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.690 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.676 |
LIG_SUMO_SIM_anti_2 | 206 | 211 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 549 | 556 | PF11976 | 0.719 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 553 | 558 | PF11976 | 0.721 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.540 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.617 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.564 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.527 |
LIG_UBA3_1 | 350 | 355 | PF00899 | 0.261 |
LIG_UBA3_1 | 365 | 370 | PF00899 | 0.261 |
MOD_CDK_SPK_2 | 124 | 129 | PF00069 | 0.509 |
MOD_CDK_SPxxK_3 | 373 | 380 | PF00069 | 0.525 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.677 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.407 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.544 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.331 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.421 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.759 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.497 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.666 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.559 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.782 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.367 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.261 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.290 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.496 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.773 |
MOD_Cter_Amidation | 410 | 413 | PF01082 | 0.554 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.677 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.696 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.770 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.465 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.501 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.601 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.655 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.512 |
MOD_GlcNHglycan | 475 | 479 | PF01048 | 0.581 |
MOD_GlcNHglycan | 531 | 537 | PF01048 | 0.606 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.570 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.558 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.693 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.648 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.390 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.433 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.353 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.403 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.411 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.261 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.489 |
MOD_N-GLC_2 | 165 | 167 | PF02516 | 0.500 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.742 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.328 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.411 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.618 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.773 |
MOD_PK_1 | 194 | 200 | PF00069 | 0.261 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.548 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.678 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.308 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.612 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.552 |
MOD_PKB_1 | 503 | 511 | PF00069 | 0.440 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.782 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.546 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.558 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.501 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.284 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.290 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.618 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.513 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.520 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.718 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.532 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.509 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.719 |
TRG_DiLeu_BaEn_2 | 563 | 569 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF4 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IB69 | Leishmania donovani | 69% | 100% |
A4HUT5 | Leishmania infantum | 69% | 100% |
E9ANG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4QH57 | Leishmania major | 68% | 100% |