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 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 3 |
GO:0032259 | methylation | 2 | 2 |
GO:0006790 | sulfur compound metabolic process | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
GO:0005488 | binding | 1 | 1 |
GO:0005542 | folic acid binding | 3 | 1 |
GO:0019842 | vitamin binding | 3 | 1 |
GO:0031406 | carboxylic acid binding | 4 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0043177 | organic acid binding | 3 | 1 |
GO:0072341 | modified amino acid binding | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0004047 | aminomethyltransferase activity | 5 | 1 |
GO:0016742 | hydroxymethyl-, formyl- and related transferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.375 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.489 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.646 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.622 |
DOC_ANK_TNKS_1 | 234 | 241 | PF00023 | 0.493 |
DOC_CYCLIN_RxL_1 | 245 | 253 | PF00134 | 0.420 |
DOC_MAPK_DCC_7 | 354 | 364 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 285 | 293 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 354 | 364 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 95 | 102 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 285 | 293 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 357 | 364 | PF00069 | 0.343 |
DOC_PP1_RVXF_1 | 258 | 265 | PF00149 | 0.391 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.398 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.366 |
DOC_USP7_UBL2_3 | 381 | 385 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.517 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 285 | 290 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 335 | 352 | PF00022 | 0.406 |
LIG_APCC_ABBAyCdc20_2 | 97 | 103 | PF00400 | 0.523 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.424 |
LIG_EVH1_2 | 204 | 208 | PF00568 | 0.425 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.493 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.375 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.382 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.606 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.572 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.357 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.449 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 226 | 233 | PF02991 | 0.469 |
LIG_LIR_LC3C_4 | 108 | 111 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.309 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.369 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 269 | 272 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.454 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.735 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.646 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.670 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.636 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 74 | 81 | PF11976 | 0.437 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.509 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.709 |
LIG_UBA3_1 | 346 | 354 | PF00899 | 0.489 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.429 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.734 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.694 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.742 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.689 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.480 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.660 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.732 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.734 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.663 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.529 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.455 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.389 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.689 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.621 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.561 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.501 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.416 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.633 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.551 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.551 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.548 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.431 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.450 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.355 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.431 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.751 |
MOD_PKA_1 | 285 | 291 | PF00069 | 0.381 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.730 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.684 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.597 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.455 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.412 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.513 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.526 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.454 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.352 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.429 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.705 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.692 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.518 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.584 |
MOD_SUMO_rev_2 | 376 | 386 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 89 | 96 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 382 | 387 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.393 |
TRG_NLS_MonoExtN_4 | 95 | 101 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM11 | Leptomonas seymouri | 62% | 89% |
A0A0S4JL83 | Bodo saltans | 39% | 100% |
A0A3R7K245 | Trypanosoma rangeli | 47% | 100% |
A2R472 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 28% | 88% |
A4HDN4 | Leishmania braziliensis | 77% | 100% |
A4R8F9 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 27% | 100% |
C9ZWC9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AH81 | Leishmania infantum | 98% | 100% |
E9AX19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4P7A4 | Ustilago maydis (strain 521 / FGSC 9021) | 27% | 97% |
Q4QAF7 | Leishmania major | 86% | 94% |
Q54NS1 | Dictyostelium discoideum | 26% | 96% |
Q6C8Y7 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 82% |
Q7RYZ1 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 89% |
Q8CAK1 | Mus musculus | 30% | 100% |
V5AJ90 | Trypanosoma cruzi | 47% | 100% |