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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QE07
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0033615 | mitochondrial proton-transporting ATP synthase complex assembly | 8 | 2 |
GO:0043461 | proton-transporting ATP synthase complex assembly | 7 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0070071 | proton-transporting two-sector ATPase complex assembly | 6 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.410 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.304 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.303 |
CLV_Separin_Metazoa | 11 | 15 | PF03568 | 0.561 |
CLV_Separin_Metazoa | 290 | 294 | PF03568 | 0.481 |
DEG_APCC_DBOX_1 | 194 | 202 | PF00400 | 0.381 |
DEG_SCF_FBW7_1 | 184 | 191 | PF00400 | 0.538 |
DOC_ANK_TNKS_1 | 176 | 183 | PF00023 | 0.411 |
DOC_CKS1_1 | 128 | 133 | PF01111 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 221 | 227 | PF00134 | 0.323 |
DOC_MAPK_gen_1 | 40 | 49 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.303 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.303 |
DOC_PP2B_LxvP_1 | 221 | 224 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.303 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.303 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 25 | 33 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.531 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.495 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.450 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.412 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.337 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.349 |
LIG_IBAR_NPY_1 | 204 | 206 | PF08397 | 0.326 |
LIG_PDZ_Class_3 | 299 | 304 | PF00595 | 0.613 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.300 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.373 |
LIG_SH3_5 | 131 | 135 | PF00018 | 0.303 |
LIG_SUMO_SIM_anti_2 | 53 | 58 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 223 | 229 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 81 | 90 | PF11976 | 0.410 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.680 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.290 |
MOD_CDK_SPK_2 | 127 | 132 | PF00069 | 0.412 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.593 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.448 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.659 |
MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.303 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.330 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.515 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.650 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.298 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.538 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.555 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.452 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.600 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.354 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.306 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.528 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.360 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.303 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.390 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.546 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.483 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.499 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.538 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.545 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.293 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.331 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.496 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.380 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.497 |
MOD_SUMO_rev_2 | 2 | 9 | PF00179 | 0.388 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E1 | Leptomonas seymouri | 87% | 78% |
A0A1X0P7M1 | Trypanosomatidae | 66% | 78% |
A0A3R7KUB6 | Trypanosoma rangeli | 65% | 78% |
A0A3S7WUT0 | Leishmania donovani | 97% | 100% |
A4H9D9 | Leishmania braziliensis | 92% | 80% |
A4HXR0 | Leishmania infantum | 97% | 100% |
B6DTF4 | Bodo saltans | 64% | 80% |
D0A042 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 80% |
E9ARH2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q1LZ96 | Bos taurus | 25% | 100% |
Q8N5M1 | Homo sapiens | 25% | 100% |
Q91YY4 | Mus musculus | 26% | 100% |
V5BRM9 | Trypanosoma cruzi | 64% | 78% |