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: A4HCX6
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 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
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 | 413 | 417 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.353 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.396 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.638 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.528 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.449 |
DOC_CKS1_1 | 311 | 316 | PF01111 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 160 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 208 | PF00134 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 10 | 21 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 387 | 395 | PF00069 | 0.233 |
DOC_MAPK_RevD_3 | 7 | 23 | PF00069 | 0.435 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.500 |
DOC_PP2B_LxvP_1 | 78 | 81 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.488 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.657 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 335 | 340 | PF00244 | 0.385 |
LIG_Actin_WH2_2 | 155 | 171 | PF00022 | 0.608 |
LIG_AP2alpha_1 | 332 | 336 | PF02296 | 0.492 |
LIG_APCC_ABBA_1 | 93 | 98 | PF00400 | 0.330 |
LIG_BIR_III_2 | 374 | 378 | PF00653 | 0.522 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.498 |
LIG_eIF4E_1 | 96 | 102 | PF01652 | 0.271 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.392 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.500 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.407 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.443 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.507 |
LIG_HCF-1_HBM_1 | 41 | 44 | PF13415 | 0.450 |
LIG_Integrin_RGD_1 | 232 | 234 | PF01839 | 0.473 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.318 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.492 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.419 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.351 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.721 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.471 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.538 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.321 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.364 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.560 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.543 |
LIG_SH3_4 | 144 | 151 | PF00018 | 0.484 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 308 | 313 | PF11976 | 0.417 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.677 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.352 |
LIG_TYR_ITIM | 90 | 95 | PF00017 | 0.371 |
LIG_UBA3_1 | 18 | 26 | PF00899 | 0.491 |
LIG_WW_3 | 353 | 357 | PF00397 | 0.491 |
MOD_CDK_SPK_2 | 287 | 292 | PF00069 | 0.494 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.735 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.729 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.534 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.534 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.312 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.720 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.662 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.521 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.680 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.397 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.466 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.363 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.623 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.639 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.736 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.550 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.609 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.199 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.629 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.644 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.363 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.481 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.533 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.213 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.477 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.491 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.336 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.533 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.554 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.364 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.580 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.500 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.417 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.360 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.633 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.731 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.242 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.664 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.393 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 386 | 389 | PF00179 | 0.254 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K4 | Leptomonas seymouri | 41% | 100% |
A0A1X0NWU1 | Trypanosomatidae | 27% | 100% |
A0A3Q8IEK9 | Leishmania donovani | 72% | 100% |
A0A3R7KPU1 | Trypanosoma rangeli | 28% | 100% |
A4I0F9 | Leishmania infantum | 72% | 100% |
C9ZV81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AWC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QB50 | Leishmania major | 71% | 100% |
V5DFL5 | Trypanosoma cruzi | 29% | 100% |