Translation, Peptide deformylase
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: A4HS79
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 11 |
GO:0006508 | proteolysis | 4 | 6 |
GO:0006518 | peptide metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 11 |
GO:0043043 | peptide biosynthetic process | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043603 | amide metabolic process | 3 | 11 |
GO:0043604 | amide biosynthetic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018206 | peptidyl-methionine modification | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 6 |
GO:0008237 | metallopeptidase activity | 4 | 6 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 11 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 11 |
GO:0042586 | peptide deformylase activity | 5 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.139 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.203 |
DEG_APCC_DBOX_1 | 254 | 262 | PF00400 | 0.270 |
DEG_APCC_DBOX_1 | 344 | 352 | PF00400 | 0.453 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.683 |
DOC_ANK_TNKS_1 | 92 | 99 | PF00023 | 0.584 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.471 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.270 |
DOC_MAPK_RevD_3 | 256 | 272 | PF00069 | 0.270 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.578 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.270 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.379 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 45 | 53 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.598 |
LIG_BIR_III_2 | 318 | 322 | PF00653 | 0.399 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.256 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.563 |
LIG_EVH1_2 | 311 | 315 | PF00568 | 0.359 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.449 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.342 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.225 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.202 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.256 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.270 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.379 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.641 |
LIG_Integrin_RGD_1 | 375 | 377 | PF01839 | 0.739 |
LIG_LIR_Apic_2 | 169 | 174 | PF02991 | 0.280 |
LIG_LIR_Apic_2 | 307 | 312 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 283 | 290 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.336 |
LIG_LYPXL_yS_3 | 105 | 108 | PF13949 | 0.474 |
LIG_LYPXL_yS_3 | 148 | 151 | PF13949 | 0.256 |
LIG_LYPXL_yS_3 | 295 | 298 | PF13949 | 0.337 |
LIG_Pex14_1 | 116 | 120 | PF04695 | 0.347 |
LIG_Pex14_1 | 291 | 295 | PF04695 | 0.368 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.397 |
LIG_Rb_pABgroove_1 | 160 | 168 | PF01858 | 0.256 |
LIG_REV1ctd_RIR_1 | 40 | 49 | PF16727 | 0.600 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.354 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.185 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.372 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.271 |
LIG_SH2_SRC | 95 | 98 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.520 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.543 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.498 |
LIG_SUMO_SIM_par_1 | 245 | 250 | PF11976 | 0.409 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.531 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.302 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.398 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.662 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.523 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.647 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.570 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.350 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.402 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.710 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.599 |
MOD_GlcNHglycan | 383 | 389 | PF01048 | 0.734 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.453 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.650 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.700 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.402 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.214 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.314 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.596 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.528 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.588 |
MOD_LATS_1 | 241 | 247 | PF00433 | 0.302 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.578 |
MOD_N-GLC_2 | 13 | 15 | PF02516 | 0.574 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.296 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.321 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.540 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.402 |
MOD_PK_1 | 56 | 62 | PF00069 | 0.642 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.319 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.402 |
MOD_Plk_2-3 | 294 | 300 | PF00069 | 0.338 |
MOD_Plk_2-3 | 377 | 383 | PF00069 | 0.604 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.256 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.402 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.364 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.689 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.319 |
MOD_SUMO_rev_2 | 192 | 201 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 322 | 330 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 131 | 136 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.181 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 202 | 207 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P349 | Leptomonas seymouri | 79% | 94% |
A0A0S4JJP7 | Bodo saltans | 46% | 100% |
A0A1X0NLE7 | Trypanosomatidae | 59% | 100% |
A0A3S5IQR8 | Trypanosoma rangeli | 64% | 100% |
A0A3S7WNT3 | Leishmania donovani | 100% | 96% |
C9ZY73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9AK65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q9U112 | Leishmania major | 92% | 100% |
V5BDN2 | Trypanosoma cruzi | 59% | 100% |