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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HNL7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0042276 | error-prone translesion synthesis | 8 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0070987 | error-free translesion synthesis | 8 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003684 | damaged DNA binding | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016779 | nucleotidyltransferase activity | 4 | 2 |
GO:0017125 | deoxycytidyl transferase activity | 5 | 1 |
GO:0034061 | DNA polymerase activity | 4 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 281 | 285 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 571 | 573 | PF00082 | 0.292 |
CLV_PCSK_PC7_1 | 289 | 295 | PF00082 | 0.434 |
CLV_PCSK_PC7_1 | 321 | 327 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.224 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.342 |
DEG_APCC_DBOX_1 | 586 | 594 | PF00400 | 0.497 |
DOC_CYCLIN_RxL_1 | 188 | 197 | PF00134 | 0.498 |
DOC_CYCLIN_RxL_1 | 349 | 356 | PF00134 | 0.340 |
DOC_CYCLIN_yCln2_LP_2 | 617 | 623 | PF00134 | 0.409 |
DOC_MAPK_DCC_7 | 422 | 430 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 141 | 151 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 393 | 401 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 509 | 519 | PF00069 | 0.658 |
DOC_MAPK_MEF2A_6 | 393 | 401 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 61 | 68 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 146 | 152 | PF00149 | 0.384 |
DOC_PP1_RVXF_1 | 25 | 31 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 617 | 620 | PF13499 | 0.432 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.571 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.396 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.625 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 373 | 377 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 472 | 477 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.643 |
LIG_Actin_WH2_2 | 229 | 244 | PF00022 | 0.498 |
LIG_Actin_WH2_2 | 448 | 466 | PF00022 | 0.549 |
LIG_APCC_ABBA_1 | 46 | 51 | PF00400 | 0.467 |
LIG_APCC_ABBAyCdc20_2 | 61 | 67 | PF00400 | 0.441 |
LIG_CaM_IQ_9 | 19 | 35 | PF13499 | 0.349 |
LIG_CaM_IQ_9 | 276 | 291 | PF13499 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 44 | 52 | PF00928 | 0.411 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.537 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.452 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.509 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.639 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.536 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.510 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.350 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.750 |
LIG_GBD_Chelix_1 | 368 | 376 | PF00786 | 0.470 |
LIG_LIR_Apic_2 | 594 | 599 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 604 | 613 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 81 | 90 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 62 | 66 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 81 | 85 | PF02991 | 0.431 |
LIG_LYPXL_yS_3 | 579 | 582 | PF13949 | 0.487 |
LIG_PDZ_Class_3 | 619 | 624 | PF00595 | 0.530 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.339 |
LIG_Pex14_2 | 42 | 46 | PF04695 | 0.336 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.466 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.535 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 118 | 121 | PF00017 | 0.442 |
LIG_SH2_SRC | 118 | 121 | PF00017 | 0.442 |
LIG_SH2_SRC | 243 | 246 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.372 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.346 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.340 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 412 | 418 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 515 | 523 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.423 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.358 |
LIG_TYR_ITIM | 577 | 582 | PF00017 | 0.483 |
LIG_TYR_ITSM | 143 | 150 | PF00017 | 0.535 |
LIG_TYR_ITSM | 296 | 303 | PF00017 | 0.401 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.518 |
LIG_WRC_WIRS_1 | 609 | 614 | PF05994 | 0.464 |
MOD_CDK_SPxxK_3 | 520 | 527 | PF00069 | 0.469 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.530 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.285 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.453 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.503 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.442 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.487 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.570 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.476 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.330 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.410 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.440 |
MOD_Cter_Amidation | 291 | 294 | PF01082 | 0.432 |
MOD_Cter_Amidation | 323 | 326 | PF01082 | 0.521 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.359 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.677 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.554 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.391 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.474 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.477 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.398 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.467 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.391 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.657 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.558 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.451 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.447 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.492 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.472 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.341 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.447 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.445 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.542 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.470 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.579 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.605 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.442 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.625 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.432 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.409 |
MOD_PK_1 | 326 | 332 | PF00069 | 0.454 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.455 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.285 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.489 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.448 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.435 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.351 |
MOD_Plk_2-3 | 163 | 169 | PF00069 | 0.431 |
MOD_Plk_2-3 | 515 | 521 | PF00069 | 0.622 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.524 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.490 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.344 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.685 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.498 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.626 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.358 |
MOD_SUMO_for_1 | 78 | 81 | PF00179 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.475 |
TRG_NES_CRM1_1 | 67 | 81 | PF08389 | 0.431 |
TRG_NLS_MonoCore_2 | 508 | 513 | PF00514 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.187 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA19 | Leptomonas seymouri | 69% | 100% |
A0A0S4JRX6 | Bodo saltans | 44% | 87% |
A0A1X0P8Q5 | Trypanosomatidae | 49% | 99% |
A0A3S7XA64 | Leishmania donovani | 82% | 100% |
A0A422NAZ8 | Trypanosoma rangeli | 48% | 100% |
A4ICX7 | Leishmania infantum | 82% | 100% |
D0A2H2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ASC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q268 | Leishmania major | 82% | 100% |
V5BV86 | Trypanosoma cruzi | 49% | 100% |