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 | 2 |
GO:0020023 | kinetoplast | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCM8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.568 |
CLV_PCSK_FUR_1 | 243 | 247 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 167 | 173 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.701 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.506 |
DOC_MAPK_gen_1 | 125 | 134 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.587 |
DOC_MAPK_RevD_3 | 158 | 172 | PF00069 | 0.651 |
DOC_MAPK_RevD_3 | 280 | 295 | PF00069 | 0.522 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.712 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.705 |
LIG_14-3-3_CanoR_1 | 128 | 132 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 187 | 204 | PF00022 | 0.535 |
LIG_APCC_ABBA_1 | 262 | 267 | PF00400 | 0.369 |
LIG_BIR_III_2 | 184 | 188 | PF00653 | 0.535 |
LIG_Clathr_ClatBox_1 | 71 | 75 | PF01394 | 0.505 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.645 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.550 |
LIG_FXI_DFP_1 | 272 | 276 | PF00024 | 0.504 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 231 | 239 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.599 |
LIG_NRBOX | 39 | 45 | PF00104 | 0.577 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.387 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.490 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.389 |
LIG_SUMO_SIM_anti_2 | 203 | 211 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 219 | 225 | PF11976 | 0.527 |
LIG_SUMO_SIM_anti_2 | 267 | 274 | PF11976 | 0.566 |
LIG_SUMO_SIM_anti_2 | 286 | 292 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 70 | 76 | PF11976 | 0.593 |
LIG_UBA3_1 | 287 | 295 | PF00899 | 0.569 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.527 |
MOD_CDK_SPK_2 | 170 | 175 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.559 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.709 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.456 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.568 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.566 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.503 |
MOD_GlcNHglycan | 217 | 221 | PF01048 | 0.502 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.486 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.461 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.365 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.623 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.735 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.635 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.476 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.595 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.450 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.507 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.497 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.613 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.741 |
MOD_PK_1 | 202 | 208 | PF00069 | 0.592 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.645 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.545 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.580 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.493 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.355 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.515 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.638 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.510 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.486 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.563 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.640 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.578 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.705 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB90 | Leptomonas seymouri | 62% | 100% |
A0A1X0NW23 | Trypanosomatidae | 39% | 100% |
A0A3Q8IBV6 | Leishmania donovani | 94% | 100% |
A0A422NTN5 | Trypanosoma rangeli | 42% | 88% |
A4HZ03 | Leishmania infantum | 94% | 100% |
C9ZIL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 81% |
E9AIM2 | Leishmania braziliensis | 83% | 100% |
E9AUV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BHE7 | Trypanosoma cruzi | 39% | 80% |