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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005657 | replication fork | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0035861 | site of double-strand break | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0090734 | site of DNA damage | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E8NHQ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 16 |
GO:0006259 | DNA metabolic process | 4 | 16 |
GO:0006281 | DNA repair | 5 | 16 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0006950 | response to stress | 2 | 16 |
GO:0006974 | DNA damage response | 4 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0033554 | cellular response to stress | 3 | 16 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 16 |
GO:0046483 | heterocycle metabolic process | 3 | 16 |
GO:0050896 | response to stimulus | 1 | 16 |
GO:0051716 | cellular response to stimulus | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0090304 | nucleic acid metabolic process | 4 | 16 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 16 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 2 |
GO:0006301 | postreplication repair | 6 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019985 | translesion synthesis | 7 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0042276 | error-prone translesion synthesis | 8 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071897 | DNA biosynthetic process | 5 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 16 |
GO:0003677 | DNA binding | 4 | 16 |
GO:0003684 | damaged DNA binding | 5 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016779 | nucleotidyltransferase activity | 4 | 3 |
GO:0034061 | DNA polymerase activity | 4 | 3 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.691 |
CLV_C14_Caspase3-7 | 551 | 555 | PF00656 | 0.491 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.348 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.319 |
CLV_Separin_Metazoa | 189 | 193 | PF03568 | 0.553 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.577 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.452 |
DEG_COP1_1 | 509 | 518 | PF00400 | 0.367 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.270 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.431 |
DOC_CYCLIN_RxL_1 | 218 | 229 | PF00134 | 0.553 |
DOC_MAPK_DCC_7 | 61 | 69 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 439 | 447 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 155 | 169 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.411 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.553 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.460 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.410 |
LIG_APCC_ABBAyCdc20_2 | 236 | 242 | PF00400 | 0.482 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.472 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.479 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.553 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.480 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.414 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.520 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.335 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.522 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.466 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.484 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.423 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.452 |
LIG_LIR_Apic_2 | 280 | 286 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 313 | 318 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 79 | 85 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 427 | 436 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.486 |
LIG_PCNA_PIPBox_1 | 541 | 550 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 535 | 548 | PF02747 | 0.546 |
LIG_PTB_Apo_2 | 388 | 395 | PF02174 | 0.373 |
LIG_PTB_Apo_2 | 446 | 453 | PF02174 | 0.531 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.553 |
LIG_SH2_SRC | 128 | 131 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.452 |
LIG_SH3_1 | 82 | 88 | PF00018 | 0.527 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.492 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.468 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.479 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.516 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.527 |
LIG_SH3_4 | 266 | 273 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 408 | 415 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 417 | 424 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 594 | 599 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 613 | 619 | PF11976 | 0.453 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.298 |
LIG_WRC_WIRS_1 | 544 | 549 | PF05994 | 0.627 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.362 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.579 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.774 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.540 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.461 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.498 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.339 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.401 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.320 |
MOD_Cter_Amidation | 349 | 352 | PF01082 | 0.541 |
MOD_DYRK1A_RPxSP_1 | 355 | 359 | PF00069 | 0.469 |
MOD_GlcNHglycan | 246 | 250 | PF01048 | 0.321 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.395 |
MOD_GlcNHglycan | 276 | 280 | PF01048 | 0.311 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.417 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.481 |
MOD_GlcNHglycan | 507 | 511 | PF01048 | 0.592 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.603 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.665 |
MOD_GlcNHglycan | 576 | 580 | PF01048 | 0.634 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.655 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.283 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.329 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.287 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.353 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.634 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.701 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.685 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.269 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.372 |
MOD_LATS_1 | 437 | 443 | PF00433 | 0.240 |
MOD_LATS_1 | 537 | 543 | PF00433 | 0.531 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.214 |
MOD_N-GLC_1 | 585 | 590 | PF02516 | 0.715 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.468 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.322 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.388 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.602 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.585 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.290 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.440 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.330 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.414 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.420 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.298 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.208 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.535 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.382 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.434 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.376 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.243 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.279 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.584 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.582 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.440 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.658 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.403 |
TRG_AP2beta_CARGO_1 | 430 | 439 | PF09066 | 0.252 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_4 | 430 | 436 | PF01217 | 0.252 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.304 |
TRG_NES_CRM1_1 | 467 | 483 | PF08389 | 0.298 |
TRG_NLS_MonoExtC_3 | 350 | 355 | PF00514 | 0.569 |
TRG_NLS_MonoExtN_4 | 351 | 356 | PF00514 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 60% | 78% |
A0A0S4J2C8 | Bodo saltans | 37% | 100% |
A0A1X0NXK7 | Trypanosomatidae | 42% | 100% |
A0A3R7NDG4 | Trypanosoma rangeli | 45% | 100% |
A0A3S5H795 | Leishmania donovani | 72% | 81% |
A4HBQ9 | Leishmania braziliensis | 79% | 82% |
A4HBR0 | Leishmania braziliensis | 76% | 100% |
A4HZ61 | Leishmania infantum | 81% | 79% |
A4HZ62 | Leishmania infantum | 83% | 81% |
D0A1I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AV29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 80% |
O42917 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 71% |
Q04049 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 98% |
Q4QCF2 | Leishmania major | 83% | 100% |
Q4QCF3 | Leishmania major | 81% | 79% |
Q9JJN0 | Mus musculus | 27% | 89% |
Q9VNX1 | Drosophila melanogaster | 26% | 70% |
Q9Y253 | Homo sapiens | 27% | 87% |
V5BMZ1 | Trypanosoma cruzi | 45% | 100% |