Protein modification, leucine carboxyl methyltransferase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3Q8IGT9
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 12 |
GO:0032259 | methylation | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.383 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.373 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.338 |
DOC_PP2B_PxIxI_1 | 152 | 158 | PF00149 | 0.415 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.353 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.268 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 59 | 69 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 162 | 177 | PF00022 | 0.388 |
LIG_Actin_WH2_2 | 71 | 88 | PF00022 | 0.388 |
LIG_AP2alpha_2 | 25 | 27 | PF02296 | 0.268 |
LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.283 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.384 |
LIG_BIR_III_4 | 136 | 140 | PF00653 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 268 | 273 | PF00928 | 0.341 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.296 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.208 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.350 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.410 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.412 |
LIG_FXI_DFP_1 | 220 | 224 | PF00024 | 0.462 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 222 | 226 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 192 | 199 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 25 | 31 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.263 |
LIG_PCNA_yPIPBox_3 | 84 | 98 | PF02747 | 0.383 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.469 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.268 |
LIG_PTB_Apo_2 | 21 | 28 | PF02174 | 0.388 |
LIG_REV1ctd_RIR_1 | 28 | 37 | PF16727 | 0.325 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.314 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.287 |
LIG_SH2_GRB2like | 22 | 25 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 193 | 197 | PF00017 | 0.383 |
LIG_SH2_PTP2 | 127 | 130 | PF00017 | 0.376 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.280 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.502 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.325 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.415 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.272 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.292 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.388 |
MOD_CDK_SPxxK_3 | 287 | 294 | PF00069 | 0.311 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.327 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.414 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.386 |
MOD_CMANNOS | 270 | 273 | PF00535 | 0.328 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.354 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.394 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.270 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.274 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.416 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.283 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.330 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.378 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.353 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.268 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.415 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.495 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.258 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.261 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.345 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.277 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.392 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.297 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.235 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.161 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.268 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.415 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.378 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.303 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.268 |
TRG_DiLeu_BaEn_1 | 271 | 276 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_2 | 277 | 283 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.272 |
TRG_NES_CRM1_1 | 256 | 269 | PF08389 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBZ8 | Leptomonas seymouri | 77% | 100% |
A0A0S4JL13 | Bodo saltans | 54% | 97% |
A0A1X0P9A8 | Trypanosomatidae | 51% | 99% |
A0A422NB24 | Trypanosoma rangeli | 53% | 99% |
A4HNL5 | Leishmania braziliensis | 89% | 100% |
A4ICX9 | Leishmania infantum | 100% | 100% |
D0A2H0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
E9ASC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O94257 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 95% |
P0CO56 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 27% | 74% |
P0CO57 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 27% | 75% |
P46554 | Caenorhabditis elegans | 30% | 89% |
Q04081 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 90% |
Q3T0H0 | Bos taurus | 27% | 89% |
Q4ICG8 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 79% |
Q4Q270 | Leishmania major | 97% | 100% |
Q4WS57 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 74% |
Q5A387 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 81% |
Q5AQJ2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 77% |
Q60YU0 | Caenorhabditis briggsae | 30% | 89% |
Q6BQD2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 80% |
Q6C997 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 91% |
Q6CWW0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 89% |
Q6FUI5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 29% | 93% |
Q6P4Z6 | Rattus norvegicus | 28% | 89% |
Q759U5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 91% |
Q8VY08 | Arabidopsis thaliana | 28% | 89% |
Q9UIC8 | Homo sapiens | 28% | 89% |
V5BQK9 | Trypanosoma cruzi | 52% | 89% |