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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X1J7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 23 |
GO:0006259 | DNA metabolic process | 4 | 23 |
GO:0006281 | DNA repair | 5 | 23 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 23 |
GO:0006807 | nitrogen compound metabolic process | 2 | 23 |
GO:0006950 | response to stress | 2 | 23 |
GO:0006974 | DNA damage response | 4 | 23 |
GO:0008152 | metabolic process | 1 | 23 |
GO:0009987 | cellular process | 1 | 23 |
GO:0033554 | cellular response to stress | 3 | 23 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 23 |
GO:0043170 | macromolecule metabolic process | 3 | 23 |
GO:0044237 | cellular metabolic process | 2 | 23 |
GO:0044238 | primary metabolic process | 2 | 23 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 23 |
GO:0046483 | heterocycle metabolic process | 3 | 23 |
GO:0050896 | response to stimulus | 1 | 23 |
GO:0051716 | cellular response to stimulus | 2 | 23 |
GO:0071704 | organic substance metabolic process | 2 | 23 |
GO:0090304 | nucleic acid metabolic process | 4 | 23 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 23 |
GO:0006260 | DNA replication | 5 | 11 |
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: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 | 23 |
GO:0003677 | DNA binding | 4 | 23 |
GO:0003684 | damaged DNA binding | 5 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0016740 | transferase activity | 2 | 23 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 23 |
GO:0016779 | nucleotidyltransferase activity | 4 | 23 |
GO:0034061 | DNA polymerase activity | 4 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 23 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.746 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 550 | 552 | PF00082 | 0.698 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.157 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.716 |
DOC_CYCLIN_RxL_1 | 404 | 411 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 504 | 510 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 139 | 148 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 200 | 208 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 425 | 431 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 142 | 150 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.435 |
DOC_MAPK_RevD_3 | 146 | 161 | PF00069 | 0.243 |
DOC_PP1_RVXF_1 | 55 | 61 | PF00149 | 0.545 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.521 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.730 |
DOC_USP7_UBL2_3 | 121 | 125 | PF12436 | 0.345 |
DOC_USP7_UBL2_3 | 593 | 597 | PF12436 | 0.720 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.766 |
LIG_14-3-3_CanoR_1 | 383 | 387 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 425 | 430 | PF00244 | 0.424 |
LIG_Actin_WH2_1 | 308 | 323 | PF00022 | 0.329 |
LIG_APCC_ABBAyCdc20_2 | 143 | 149 | PF00400 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.539 |
LIG_eIF4E_1 | 350 | 356 | PF01652 | 0.393 |
LIG_eIF4E_1 | 470 | 476 | PF01652 | 0.409 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.361 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.457 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.461 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.413 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.437 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.562 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.484 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.408 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.714 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.335 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.523 |
LIG_GBD_Chelix_1 | 361 | 369 | PF00786 | 0.275 |
LIG_HCF-1_HBM_1 | 347 | 350 | PF13415 | 0.296 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 112 | 119 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 231 | 242 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 252 | 256 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.493 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.521 |
LIG_SH2_NCK_1 | 154 | 158 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 145 | 148 | PF00017 | 0.272 |
LIG_SH2_SRC | 145 | 148 | PF00017 | 0.359 |
LIG_SH2_SRC | 74 | 77 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.480 |
LIG_SH2_STAT3 | 230 | 233 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.495 |
LIG_SH3_1 | 566 | 572 | PF00018 | 0.575 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.569 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.520 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.576 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.714 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.756 |
LIG_SH3_4 | 296 | 303 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 205 | 210 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 302 | 307 | PF11976 | 0.501 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.484 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.446 |
LIG_TRAF2_2 | 507 | 512 | PF00917 | 0.513 |
LIG_UBA3_1 | 351 | 359 | PF00899 | 0.481 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.410 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.521 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.444 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.443 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.452 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.464 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.765 |
MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.252 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.526 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.324 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.292 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.242 |
MOD_GlcNHglycan | 526 | 530 | PF01048 | 0.709 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.490 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.649 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.502 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.415 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.498 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.459 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.649 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.660 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.670 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.468 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.419 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.428 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.433 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.510 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.534 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.431 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.561 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.410 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.454 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.505 |
MOD_PK_1 | 222 | 228 | PF00069 | 0.521 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.452 |
MOD_PKA_1 | 584 | 590 | PF00069 | 0.740 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.368 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.458 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.737 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.783 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.406 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.501 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.313 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.415 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.437 |
MOD_Plk_2-3 | 240 | 246 | PF00069 | 0.417 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.521 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.534 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.410 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.462 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.765 |
MOD_SUMO_rev_2 | 158 | 163 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 447 | 454 | PF00179 | 0.409 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.284 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.513 |
TRG_NES_CRM1_1 | 260 | 274 | PF08389 | 0.521 |
TRG_NLS_MonoExtC_3 | 549 | 554 | PF00514 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.279 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I6 | Leptomonas seymouri | 37% | 85% |
A0A0N1I6L1 | Leptomonas seymouri | 72% | 90% |
A0A0N1PDB9 | Leptomonas seymouri | 46% | 96% |
A0A0S4JDU0 | Bodo saltans | 38% | 67% |
A0A1X0NYM2 | Trypanosomatidae | 44% | 98% |
A0A1X0NZ35 | Trypanosomatidae | 50% | 100% |
A0A3Q8IEM0 | Leishmania donovani | 36% | 79% |
A4HGJ3 | Leishmania braziliensis | 37% | 79% |
A4I3M0 | Leishmania infantum | 37% | 79% |
A4I3M1 | Leishmania infantum | 100% | 100% |
A4I3M2 | Leishmania infantum | 39% | 100% |
D0A846 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A847 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A848 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A849 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A851 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A852 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AZW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 79% |
E9AZW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AZW3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
O74944 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
Q4Q8C4 | Leishmania major | 96% | 100% |
Q4Q8C5 | Leishmania major | 36% | 80% |
Q6JDV7 | Arabidopsis thaliana | 36% | 89% |