Proteases, methionine aminopeptidase
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HY76
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0070084 | protein initiator methionine removal | 5 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0016485 | protein processing | 5 | 1 |
GO:0035551 | protein initiator methionine removal involved in protein maturation | 6 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004177 | aminopeptidase activity | 5 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008233 | peptidase activity | 3 | 13 |
GO:0008235 | metalloexopeptidase activity | 5 | 13 |
GO:0008237 | metallopeptidase activity | 4 | 13 |
GO:0008238 | exopeptidase activity | 4 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0070006 | metalloaminopeptidase activity | 6 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.275 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.403 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.198 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.198 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.255 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.398 |
DOC_CYCLIN_RxL_1 | 16 | 26 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 382 | 391 | PF00069 | 0.422 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.433 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.358 |
DOC_USP7_MATH_2 | 392 | 398 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.269 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.401 |
LIG_Actin_WH2_2 | 58 | 75 | PF00022 | 0.517 |
LIG_deltaCOP1_diTrp_1 | 336 | 343 | PF00928 | 0.255 |
LIG_deltaCOP1_diTrp_1 | 372 | 379 | PF00928 | 0.460 |
LIG_EVH1_2 | 24 | 28 | PF00568 | 0.421 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.280 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.269 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.515 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.395 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.304 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.262 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 386 | 390 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 333 | 340 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.285 |
LIG_PDZ_Class_2 | 396 | 401 | PF00595 | 0.544 |
LIG_Pex14_2 | 34 | 38 | PF04695 | 0.421 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.269 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.305 |
LIG_SH2_GRB2like | 185 | 188 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.422 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.103 |
LIG_SH3_2 | 71 | 76 | PF14604 | 0.444 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.285 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.285 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.255 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.358 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 365 | 372 | PF11976 | 0.468 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.358 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.385 |
LIG_UBA3_1 | 135 | 139 | PF00899 | 0.398 |
LIG_UBA3_1 | 255 | 263 | PF00899 | 0.358 |
MOD_CDK_SPK_2 | 75 | 80 | PF00069 | 0.391 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.391 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.255 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.358 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.305 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.260 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.525 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.391 |
MOD_Cter_Amidation | 349 | 352 | PF01082 | 0.255 |
MOD_GlcNHglycan | 280 | 284 | PF01048 | 0.368 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.292 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.267 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.435 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.285 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.278 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.269 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.260 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.285 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.416 |
MOD_N-GLC_2 | 304 | 306 | PF02516 | 0.373 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.290 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.261 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.258 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.368 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.412 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.453 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.496 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.429 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.456 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.258 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.279 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.245 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.269 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.255 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.269 |
MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.482 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.431 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.324 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.269 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.269 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.269 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.366 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.398 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.392 |
MOD_SUMO_rev_2 | 345 | 353 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 394 | 401 | PF00179 | 0.538 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_3 | 242 | 248 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.218 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.269 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEB6 | Leptomonas seymouri | 85% | 97% |
A0A0S4IW90 | Bodo saltans | 66% | 100% |
A0A0S4IXB9 | Bodo saltans | 54% | 100% |
A0A1X0P6I6 | Trypanosomatidae | 72% | 100% |
A0A3R7P3I2 | Trypanosoma rangeli | 72% | 100% |
A0A3S7WVI9 | Leishmania donovani | 100% | 100% |
A4HA12 | Leishmania braziliensis | 93% | 100% |
A6QLA4 | Bos taurus | 53% | 100% |
D0A0J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AS06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
O59730 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
P0A5J3 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 43% | 100% |
P53582 | Homo sapiens | 52% | 100% |
P9WK18 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 43% | 100% |
P9WK19 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 43% | 100% |
Q01662 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 100% |
Q4QDG7 | Leishmania major | 98% | 100% |
Q4QRK0 | Danio rerio | 53% | 100% |
Q4VBS4 | Danio rerio | 41% | 100% |
Q54VU7 | Dictyostelium discoideum | 40% | 99% |
Q54WU3 | Dictyostelium discoideum | 51% | 100% |
Q5I0A0 | Xenopus tropicalis | 53% | 100% |
Q5RBF3 | Pongo abelii | 52% | 100% |
Q5ZIM5 | Gallus gallus | 52% | 100% |
Q6UB28 | Homo sapiens | 38% | 100% |
Q7ZWV9 | Xenopus laevis | 53% | 100% |
Q8BP48 | Mus musculus | 52% | 100% |
Q8IJP2 | Plasmodium falciparum (isolate 3D7) | 46% | 78% |
Q9CPW9 | Mus musculus | 40% | 100% |
Q9FV50 | Arabidopsis thaliana | 42% | 100% |
Q9FV51 | Arabidopsis thaliana | 41% | 100% |
Q9FV52 | Arabidopsis thaliana | 46% | 100% |
Q9SLN5 | Arabidopsis thaliana | 48% | 100% |
V5DTM6 | Trypanosoma cruzi | 72% | 100% |