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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGM9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006260 | DNA replication | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003896 | DNA primase activity | 7 | 2 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016779 | nucleotidyltransferase activity | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 2 |
GO:0097747 | RNA polymerase activity | 4 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 475 | 481 | PF00089 | 0.343 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.205 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.426 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.405 |
DOC_CYCLIN_RxL_1 | 128 | 135 | PF00134 | 0.480 |
DOC_CYCLIN_RxL_1 | 88 | 97 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 501 | 507 | PF00134 | 0.480 |
DOC_MAPK_DCC_7 | 59 | 68 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 327 | 333 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 378 | 387 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 513 | 519 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.404 |
DOC_MAPK_RevD_3 | 499 | 515 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 260 | 267 | PF00149 | 0.343 |
DOC_PP1_RVXF_1 | 513 | 520 | PF00149 | 0.330 |
DOC_PP1_RVXF_1 | 89 | 96 | PF00149 | 0.368 |
DOC_PP4_FxxP_1 | 149 | 152 | PF00568 | 0.323 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.428 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.563 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.537 |
DOC_USP7_UBL2_3 | 502 | 506 | PF12436 | 0.343 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.323 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 344 | 352 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 353 | 358 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 383 | 388 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 498 | 502 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 46 | 61 | PF00022 | 0.405 |
LIG_Actin_WH2_2 | 490 | 508 | PF00022 | 0.480 |
LIG_AP2alpha_1 | 149 | 153 | PF02296 | 0.443 |
LIG_AP2alpha_2 | 151 | 153 | PF02296 | 0.443 |
LIG_APCC_ABBA_1 | 92 | 97 | PF00400 | 0.443 |
LIG_APCC_ABBAyCdc20_2 | 91 | 97 | PF00400 | 0.443 |
LIG_BIR_III_2 | 371 | 375 | PF00653 | 0.438 |
LIG_BIR_III_4 | 436 | 440 | PF00653 | 0.564 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 494 | 499 | PF00928 | 0.343 |
LIG_eIF4E_1 | 269 | 275 | PF01652 | 0.368 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.362 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.445 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.569 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.518 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.610 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.538 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.479 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.305 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.438 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.261 |
LIG_HCF-1_HBM_1 | 312 | 315 | PF13415 | 0.430 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.155 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 494 | 499 | PF02991 | 0.155 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.343 |
LIG_LYPXL_yS_3 | 84 | 87 | PF13949 | 0.443 |
LIG_Pex14_1 | 528 | 532 | PF04695 | 0.428 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.443 |
LIG_RPA_C_Fungi | 376 | 388 | PF08784 | 0.466 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.368 |
LIG_SH2_CRK | 438 | 442 | PF00017 | 0.622 |
LIG_SH2_GRB2like | 534 | 537 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.405 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.405 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.343 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 473 | 477 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 507 | 511 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 315 | 318 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.443 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.413 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.599 |
LIG_Sin3_3 | 153 | 160 | PF02671 | 0.443 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 359 | 364 | PF11976 | 0.540 |
LIG_SxIP_EBH_1 | 55 | 69 | PF03271 | 0.461 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.443 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.343 |
LIG_WW_3 | 465 | 469 | PF00397 | 0.368 |
MOD_CDC14_SPxK_1 | 503 | 506 | PF00782 | 0.443 |
MOD_CDK_SPK_2 | 257 | 262 | PF00069 | 0.427 |
MOD_CDK_SPxK_1 | 500 | 506 | PF00069 | 0.443 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.497 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.366 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.373 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.483 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.370 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.491 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.390 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.471 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.427 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.438 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.365 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.301 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.443 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.443 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.443 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.617 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.324 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.448 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.471 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.606 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.405 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.339 |
MOD_LATS_1 | 172 | 178 | PF00433 | 0.443 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.343 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.343 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.426 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.443 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.397 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.559 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.426 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.443 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.434 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.443 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.550 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.345 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.434 |
MOD_PKB_1 | 381 | 389 | PF00069 | 0.324 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.330 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.261 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.343 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.458 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.438 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.330 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.345 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.600 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.320 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.592 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.438 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.432 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.455 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.443 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.426 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.301 |
MOD_SUMO_rev_2 | 371 | 377 | PF00179 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.205 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.446 |
TRG_NLS_MonoExtN_4 | 195 | 201 | PF00514 | 0.424 |
TRG_NLS_MonoExtN_4 | 202 | 208 | PF00514 | 0.367 |
TRG_NLS_MonoExtN_4 | 378 | 385 | PF00514 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 368 | 373 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2T3 | Leptomonas seymouri | 67% | 71% |
A0A1X0NMZ0 | Trypanosomatidae | 47% | 71% |
A0A3R7JWW2 | Trypanosoma rangeli | 48% | 77% |
A0A3S7WS08 | Leishmania donovani | 94% | 100% |
A4H6X7 | Leishmania braziliensis | 81% | 94% |
E9AGF1 | Leishmania infantum | 93% | 100% |
E9ANZ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DG34 | Trypanosoma cruzi | 46% | 90% |