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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042575 | DNA polymerase complex | 3 | 12 |
GO:0043625 | delta DNA polymerase complex | 3 | 12 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
Related structures:
AlphaFold database: A4HEE9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 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: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:0006271 | DNA strand elongation involved in DNA replication | 6 | 1 |
GO:0022616 | DNA strand elongation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016779 | nucleotidyltransferase activity | 4 | 8 |
GO:0034061 | DNA polymerase activity | 4 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.361 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.297 |
CLV_Separin_Metazoa | 71 | 75 | PF03568 | 0.338 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.319 |
DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.424 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.309 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.419 |
DOC_MAPK_FxFP_2 | 442 | 445 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 228 | 237 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 252 | 261 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 273 | 280 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 313 | 322 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 346 | 355 | PF00069 | 0.315 |
DOC_MAPK_HePTP_8 | 310 | 322 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 228 | 237 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 313 | 322 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 530 | 539 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 230 | 238 | PF00069 | 0.361 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.198 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.338 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.319 |
DOC_PP4_FxxP_1 | 551 | 554 | PF00568 | 0.563 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 273 | 277 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 472 | 477 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 496 | 504 | PF00244 | 0.508 |
LIG_AP2alpha_2 | 450 | 452 | PF02296 | 0.304 |
LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.319 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.308 |
LIG_Clathr_ClatBox_1 | 534 | 538 | PF01394 | 0.374 |
LIG_Clathr_ClatBox_1 | 72 | 76 | PF01394 | 0.292 |
LIG_EH_1 | 357 | 361 | PF12763 | 0.424 |
LIG_eIF4E_1 | 55 | 61 | PF01652 | 0.338 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.304 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.306 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.340 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.424 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.419 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.458 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.420 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.329 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.465 |
LIG_LIR_Apic_2 | 440 | 445 | PF02991 | 0.319 |
LIG_LIR_Apic_2 | 550 | 554 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.387 |
LIG_MYND_1 | 341 | 345 | PF01753 | 0.319 |
LIG_NRBOX | 306 | 312 | PF00104 | 0.424 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.319 |
LIG_PTAP_UEV_1 | 434 | 439 | PF05743 | 0.304 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.416 |
LIG_SH2_STAT3 | 27 | 30 | PF00017 | 0.198 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.419 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.453 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.333 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.304 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.304 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.387 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.304 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.394 |
LIG_SUMO_SIM_anti_2 | 232 | 238 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 319 | 324 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 316 | 321 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 425 | 430 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 533 | 538 | PF11976 | 0.388 |
LIG_WRC_WIRS_1 | 525 | 530 | PF05994 | 0.377 |
LIG_WRC_WIRS_1 | 548 | 553 | PF05994 | 0.492 |
MOD_CDK_SPK_2 | 491 | 496 | PF00069 | 0.489 |
MOD_CDK_SPxxK_3 | 491 | 498 | PF00069 | 0.489 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.417 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.702 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.741 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.503 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.198 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.361 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.426 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.464 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.377 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.332 |
MOD_GlcNHglycan | 141 | 146 | PF01048 | 0.265 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.525 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.440 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.351 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.314 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.342 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.361 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.676 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.719 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.446 |
MOD_GlcNHglycan | 83 | 88 | PF01048 | 0.387 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.307 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.352 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.357 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.256 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.334 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.304 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.420 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.511 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.375 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.407 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.430 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.419 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.461 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.377 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.394 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.305 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.623 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.665 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.351 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.369 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.198 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.353 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.198 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.532 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.384 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.304 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.458 |
MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.198 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.439 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.381 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.444 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.389 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.489 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.389 |
MOD_SUMO_for_1 | 377 | 380 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 265 | 274 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 284 | 293 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 505 | 514 | PF00179 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 518 | 523 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.351 |
TRG_NES_CRM1_1 | 308 | 321 | PF08389 | 0.424 |
TRG_NLS_MonoExtC_3 | 274 | 279 | PF00514 | 0.319 |
TRG_NLS_MonoExtC_3 | 387 | 393 | PF00514 | 0.426 |
TRG_NLS_MonoExtN_4 | 273 | 280 | PF00514 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 38 | 43 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P663 | Leptomonas seymouri | 70% | 96% |
A0A0S4IRV7 | Bodo saltans | 39% | 100% |
A0A1X0NMG0 | Trypanosomatidae | 46% | 99% |
A0A3Q8ING8 | Leishmania donovani | 86% | 94% |
A0A422P247 | Trypanosoma rangeli | 46% | 99% |
A4I1I5 | Leishmania infantum | 86% | 94% |
C9ZJY3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 98% |
E9AXM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 94% |
O35654 | Mus musculus | 26% | 100% |
O48520 | Arabidopsis thaliana | 26% | 100% |
O93610 | Xenopus laevis | 27% | 100% |
P46957 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P49004 | Bos taurus | 26% | 100% |
P87324 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
Q4Q9V2 | Leishmania major | 86% | 100% |
Q6AXY4 | Rattus norvegicus | 25% | 100% |
Q9LRE5 | Oryza sativa subsp. japonica | 26% | 100% |
Q9W088 | Drosophila melanogaster | 27% | 100% |
V5B3K0 | Trypanosoma cruzi | 47% | 100% |