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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HCT9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0006261 | DNA-templated DNA replication | 6 | 1 |
GO:0006264 | mitochondrial DNA replication | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0032042 | mitochondrial DNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016779 | nucleotidyltransferase activity | 4 | 5 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 5 |
GO:0097747 | RNA polymerase activity | 4 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
GO:0003896 | DNA primase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.334 |
CLV_MEL_PAP_1 | 165 | 171 | PF00089 | 0.241 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.709 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.704 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.461 |
DEG_APCC_KENBOX_2 | 283 | 287 | PF00400 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.590 |
DEG_SCF_FBW7_2 | 204 | 210 | PF00400 | 0.384 |
DEG_SCF_FBW7_2 | 494 | 499 | PF00400 | 0.493 |
DOC_ANK_TNKS_1 | 5 | 12 | PF00023 | 0.731 |
DOC_CKS1_1 | 141 | 146 | PF01111 | 0.377 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.242 |
DOC_CKS1_1 | 204 | 209 | PF01111 | 0.379 |
DOC_CYCLIN_RxL_1 | 325 | 334 | PF00134 | 0.386 |
DOC_CYCLIN_yCln2_LP_2 | 414 | 420 | PF00134 | 0.324 |
DOC_MAPK_DCC_7 | 258 | 268 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 284 | 294 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 378 | 388 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 431 | 437 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 465 | 472 | PF00069 | 0.459 |
DOC_MAPK_HePTP_8 | 165 | 177 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 168 | 177 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 392 | 399 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 465 | 474 | PF00069 | 0.475 |
DOC_MAPK_NFAT4_5 | 392 | 400 | PF00069 | 0.295 |
DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 470 | 473 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.333 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.735 |
DOC_USP7_MATH_2 | 184 | 190 | PF00917 | 0.303 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.277 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 287 | 294 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 487 | 494 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 216 | 233 | PF00022 | 0.368 |
LIG_APCC_ABBA_1 | 291 | 296 | PF00400 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 295 | 303 | PF00928 | 0.372 |
LIG_deltaCOP1_diTrp_1 | 390 | 394 | PF00928 | 0.296 |
LIG_deltaCOP1_diTrp_1 | 443 | 449 | PF00928 | 0.277 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.466 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.463 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.402 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.495 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.461 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.602 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.666 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.405 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.412 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 331 | 335 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 324 | 332 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 443 | 454 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 443 | 449 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.277 |
LIG_MAD2 | 199 | 207 | PF02301 | 0.404 |
LIG_OCRL_FandH_1 | 248 | 260 | PF00620 | 0.430 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.359 |
LIG_Pex14_1 | 460 | 464 | PF04695 | 0.277 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.335 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.482 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.381 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.432 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.368 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.388 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.244 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.403 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.445 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 171 | 178 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 143 | 150 | PF11976 | 0.356 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.806 |
LIG_UBA3_1 | 1 | 7 | PF00899 | 0.722 |
LIG_UBA3_1 | 276 | 284 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.445 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.388 |
MOD_CDK_SPxK_1 | 203 | 209 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 101 | 108 | PF00069 | 0.381 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.348 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.428 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.613 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.575 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.605 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.512 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.656 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.603 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.683 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.420 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.412 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.647 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.692 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.683 |
MOD_CMANNOS | 391 | 394 | PF00535 | 0.277 |
MOD_DYRK1A_RPxSP_1 | 168 | 172 | PF00069 | 0.412 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.532 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.402 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.375 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.495 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.657 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.426 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.397 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.494 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.609 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.755 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.585 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.407 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.506 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.709 |
MOD_N-GLC_2 | 55 | 57 | PF02516 | 0.512 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.490 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.252 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.345 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.613 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.329 |
MOD_PKA_1 | 487 | 493 | PF00069 | 0.456 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.445 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.733 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.448 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.708 |
MOD_Plk_2-3 | 22 | 28 | PF00069 | 0.793 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.500 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.432 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.417 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.349 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.386 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.361 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.464 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.483 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 208 | 211 | PF00179 | 0.425 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.366 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.648 |
TRG_NES_CRM1_1 | 213 | 226 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 328 | 333 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 6 | 10 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R5 | Leptomonas seymouri | 67% | 77% |
A0A0S4IY41 | Bodo saltans | 44% | 100% |
A0A1X0NXL3 | Trypanosomatidae | 52% | 85% |
A0A3S7WXR7 | Leishmania donovani | 83% | 100% |
A4I0B9 | Leishmania infantum | 82% | 78% |
C9ZV17 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 85% |
E9AW83 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QB95 | Leishmania major | 81% | 99% |
V5D725 | Trypanosoma cruzi | 61% | 86% |