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: E9AK65
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 11 |
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 |
GO:0006508 | proteolysis | 4 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
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:0008233 | peptidase activity | 3 | 5 |
GO:0008237 | metallopeptidase activity | 4 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.300 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.301 |
DEG_APCC_DBOX_1 | 262 | 270 | PF00400 | 0.338 |
DEG_APCC_DBOX_1 | 352 | 360 | PF00400 | 0.619 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.696 |
DOC_ANK_TNKS_1 | 100 | 107 | PF00023 | 0.627 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.483 |
DOC_MAPK_gen_1 | 259 | 266 | PF00069 | 0.338 |
DOC_MAPK_RevD_3 | 264 | 280 | PF00069 | 0.338 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.743 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.338 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.186 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.630 |
DOC_USP7_UBL2_3 | 369 | 373 | PF12436 | 0.611 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.362 |
LIG_14-3-3_CanoR_1 | 17 | 26 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 2 | 9 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 237 | 242 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.186 |
LIG_14-3-3_CanoR_1 | 309 | 313 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 322 | 329 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 88 | 96 | PF00244 | 0.492 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.731 |
LIG_EVH1_2 | 319 | 323 | PF00568 | 0.429 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.488 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.292 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.373 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.317 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.338 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.444 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.589 |
LIG_Integrin_RGD_1 | 383 | 385 | PF01839 | 0.701 |
LIG_LIR_Apic_2 | 177 | 182 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 291 | 298 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 311 | 321 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.414 |
LIG_LYPXL_S_1 | 112 | 116 | PF13949 | 0.186 |
LIG_LYPXL_yS_3 | 113 | 116 | PF13949 | 0.443 |
LIG_LYPXL_yS_3 | 156 | 159 | PF13949 | 0.322 |
LIG_LYPXL_yS_3 | 303 | 306 | PF13949 | 0.409 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.338 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.438 |
LIG_PTB_Apo_2 | 173 | 180 | PF02174 | 0.440 |
LIG_Rb_pABgroove_1 | 168 | 176 | PF01858 | 0.322 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.484 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.322 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.438 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.591 |
LIG_SH2_SRC | 154 | 157 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.352 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.659 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.560 |
LIG_SUMO_SIM_par_1 | 253 | 258 | PF11976 | 0.447 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.591 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.478 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.476 |
LIG_WRC_WIRS_1 | 55 | 60 | PF05994 | 0.601 |
MOD_CDK_SPxxK_3 | 315 | 322 | PF00069 | 0.255 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.713 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.450 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.707 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.578 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.186 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.551 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.391 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.443 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.644 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.739 |
MOD_GlcNHglycan | 392 | 397 | PF01048 | 0.532 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.688 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.647 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.513 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.443 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.719 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.380 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.740 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.598 |
MOD_LATS_1 | 249 | 255 | PF00433 | 0.443 |
MOD_LATS_1 | 87 | 93 | PF00433 | 0.453 |
MOD_N-GLC_2 | 28 | 30 | PF02516 | 0.732 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.657 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.338 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.388 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.642 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.186 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.443 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.457 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.672 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.186 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.384 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.743 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.443 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.577 |
MOD_Plk_2-3 | 302 | 308 | PF00069 | 0.410 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.320 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.443 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.375 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.712 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.729 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 200 | 209 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 330 | 338 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 139 | 144 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P349 | Leptomonas seymouri | 80% | 96% |
A0A0S4JJP7 | Bodo saltans | 45% | 100% |
A0A1X0NLE7 | Trypanosomatidae | 62% | 100% |
A0A3S5IQR8 | Trypanosoma rangeli | 64% | 100% |
A0A3S7WNT3 | Leishmania donovani | 89% | 98% |
A4HS79 | Leishmania infantum | 89% | 100% |
C9ZY73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
Q9U112 | Leishmania major | 88% | 100% |
V5BDN2 | Trypanosoma cruzi | 64% | 100% |