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: A4H9D9
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: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 |
GO:0033615 | mitochondrial proton-transporting ATP synthase complex assembly | 8 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.616 |
CLV_Separin_Metazoa | 368 | 372 | PF03568 | 0.471 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.391 |
DEG_SCF_FBW7_1 | 262 | 269 | PF00400 | 0.557 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.704 |
DOC_ANK_TNKS_1 | 254 | 261 | PF00023 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 299 | 305 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 118 | 127 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 155 | 165 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 124 | 130 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.328 |
DOC_PP2B_LxvP_1 | 188 | 191 | PF13499 | 0.328 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.354 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.400 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.383 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.513 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.513 |
LIG_eIF4E_1 | 184 | 190 | PF01652 | 0.314 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.475 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.347 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.375 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.585 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.523 |
LIG_IBAR_NPY_1 | 282 | 284 | PF08397 | 0.345 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 334 | 344 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.334 |
LIG_PDZ_Class_3 | 377 | 382 | PF00595 | 0.621 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 184 | 187 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 178 | 181 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 184 | 187 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.328 |
LIG_SH3_1 | 55 | 61 | PF00018 | 0.614 |
LIG_SH3_2 | 37 | 42 | PF14604 | 0.568 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.389 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.558 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.520 |
LIG_SH3_5 | 209 | 213 | PF00018 | 0.328 |
LIG_SUMO_SIM_anti_2 | 131 | 136 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 133 | 139 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 159 | 168 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 301 | 307 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.371 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.674 |
LIG_WRC_WIRS_1 | 214 | 219 | PF05994 | 0.328 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.606 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.558 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.556 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.367 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.479 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.506 |
MOD_Cter_Amidation | 150 | 153 | PF01082 | 0.328 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.550 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.319 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.298 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.537 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.323 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.262 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.565 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.439 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.652 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.488 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.614 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.655 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.563 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.385 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.414 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.330 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.597 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.715 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.328 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.421 |
MOD_PKA_1 | 42 | 48 | PF00069 | 0.552 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.586 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.552 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.389 |
MOD_PKB_1 | 41 | 49 | PF00069 | 0.681 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.531 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.564 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.584 |
MOD_Plk_2-3 | 323 | 329 | PF00069 | 0.576 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.528 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.322 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.354 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.610 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 68 | 76 | PF00179 | 0.493 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.548 |
TRG_NLS_MonoCore_2 | 37 | 42 | PF00514 | 0.553 |
TRG_NLS_MonoExtC_3 | 37 | 42 | PF00514 | 0.553 |
TRG_NLS_MonoExtN_4 | 37 | 42 | PF00514 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E1 | Leptomonas seymouri | 83% | 98% |
A0A1X0P7M1 | Trypanosomatidae | 67% | 98% |
A0A3R7KUB6 | Trypanosoma rangeli | 64% | 98% |
A0A3S7WUT0 | Leishmania donovani | 92% | 100% |
A4HXR0 | Leishmania infantum | 92% | 100% |
B6DTF4 | Bodo saltans | 65% | 100% |
D0A042 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ARH2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QE07 | Leishmania major | 92% | 100% |
V5BRM9 | Trypanosoma cruzi | 65% | 97% |