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:0005739 | mitochondrion | 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: A0A3Q8IEK9
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006730 | one-carbon metabolic process | 3 | 1 |
GO:0006760 | folic acid-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009396 | folic acid-containing compound biosynthetic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035999 | tetrahydrofolate interconversion | 4 | 1 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 1 |
GO:0042558 | pteridine-containing compound metabolic process | 4 | 1 |
GO:0042559 | pteridine-containing compound biosynthetic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046653 | tetrahydrofolate metabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016882 | cyclo-ligase activity | 4 | 1 |
GO:0030272 | 5-formyltetrahydrofolate cyclo-ligase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.383 |
CLV_MEL_PAP_1 | 353 | 359 | PF00089 | 0.610 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.403 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.624 |
DEG_SPOP_SBC_1 | 148 | 152 | PF00917 | 0.667 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.525 |
DOC_CKS1_1 | 118 | 123 | PF01111 | 0.457 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 208 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.505 |
DOC_MAPK_DCC_7 | 135 | 144 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 10 | 21 | PF00069 | 0.504 |
DOC_MAPK_HePTP_8 | 132 | 144 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 135 | 144 | PF00069 | 0.715 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.472 |
DOC_MAPK_RevD_3 | 7 | 23 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.581 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.454 |
DOC_PP2B_PxIxI_1 | 409 | 415 | PF00149 | 0.538 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.357 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.688 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 401 | 410 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 430 | 436 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 60 | 67 | PF00244 | 0.655 |
LIG_Actin_WH2_2 | 386 | 403 | PF00022 | 0.357 |
LIG_AP2alpha_1 | 332 | 336 | PF02296 | 0.492 |
LIG_APCC_ABBA_1 | 92 | 97 | PF00400 | 0.334 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.518 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.398 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.411 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.592 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.513 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.420 |
LIG_HCF-1_HBM_1 | 41 | 44 | PF13415 | 0.449 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 41 | 51 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.321 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.492 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.419 |
LIG_SH2_SRC | 44 | 47 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.351 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.369 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.729 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.329 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.471 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.481 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.409 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.487 |
LIG_SUMO_SIM_par_1 | 120 | 127 | PF11976 | 0.371 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.375 |
LIG_UBA3_1 | 18 | 26 | PF00899 | 0.496 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.612 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.676 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.575 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.654 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.638 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.281 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.689 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.555 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.614 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.404 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.505 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.556 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.482 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.664 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.506 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.749 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.502 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.602 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.623 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.656 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.393 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.509 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.652 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.527 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.486 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.508 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.503 |
MOD_PK_1 | 106 | 112 | PF00069 | 0.536 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.557 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.577 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.687 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.397 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.523 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.552 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.577 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.342 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.532 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.535 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.428 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.361 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.584 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.652 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.503 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.429 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.565 |
MOD_SUMO_for_1 | 25 | 28 | PF00179 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.464 |
TRG_ER_FFAT_1 | 273 | 284 | PF00635 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 346 | 351 | PF00026 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K4 | Leptomonas seymouri | 41% | 100% |
A0A1X0NWU1 | Trypanosomatidae | 27% | 100% |
A0A3R7KPU1 | Trypanosoma rangeli | 26% | 100% |
A4HCX6 | Leishmania braziliensis | 72% | 100% |
A4I0F9 | Leishmania infantum | 100% | 100% |
C9ZV81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AWC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QB50 | Leishmania major | 90% | 100% |
V5DFL5 | Trypanosoma cruzi | 29% | 100% |