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 | 1 |
GO:0020023 | kinetoplast | 2 | 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: E9AIK0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 332 | 338 | PF00089 | 0.452 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 247 | 251 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.352 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.333 |
DEG_COP1_1 | 265 | 275 | PF00400 | 0.458 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.525 |
DEG_SCF_FBW7_1 | 279 | 286 | PF00400 | 0.364 |
DOC_CDC14_PxL_1 | 269 | 277 | PF14671 | 0.351 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.301 |
DOC_CYCLIN_yCln2_LP_2 | 196 | 202 | PF00134 | 0.355 |
DOC_MAPK_DCC_7 | 161 | 171 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.355 |
DOC_PP4_MxPP_1 | 98 | 101 | PF00568 | 0.423 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.525 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 300 | 307 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.328 |
LIG_Clathr_ClatBox_1 | 169 | 173 | PF01394 | 0.501 |
LIG_DLG_GKlike_1 | 251 | 259 | PF00625 | 0.485 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.459 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.297 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.453 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.412 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.496 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.255 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.589 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 142 | 153 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 267 | 277 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.617 |
LIG_MYND_1 | 273 | 277 | PF01753 | 0.313 |
LIG_NRBOX | 184 | 190 | PF00104 | 0.473 |
LIG_PCNA_PIPBox_1 | 181 | 190 | PF02747 | 0.402 |
LIG_Pex14_1 | 248 | 252 | PF04695 | 0.635 |
LIG_Pex14_2 | 334 | 338 | PF04695 | 0.455 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.478 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.516 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.399 |
LIG_SH2_GRB2like | 144 | 147 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.513 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.459 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.442 |
LIG_SH3_5 | 140 | 144 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 167 | 173 | PF11976 | 0.489 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 167 | 173 | PF11976 | 0.508 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.404 |
LIG_TRFH_1 | 145 | 149 | PF08558 | 0.478 |
LIG_TRFH_1 | 269 | 273 | PF08558 | 0.384 |
LIG_TYR_ITIM | 202 | 207 | PF00017 | 0.443 |
LIG_TYR_ITIM | 231 | 236 | PF00017 | 0.472 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.437 |
MOD_CDK_SPK_2 | 136 | 141 | PF00069 | 0.449 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.420 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.552 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.461 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.566 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.675 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.488 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.278 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.540 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.530 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.405 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.526 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.652 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.351 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.355 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.369 |
MOD_N-GLC_2 | 302 | 304 | PF02516 | 0.270 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.505 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.570 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.491 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.629 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.398 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.398 |
MOD_PKA_1 | 190 | 196 | PF00069 | 0.307 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.307 |
MOD_PKB_1 | 249 | 257 | PF00069 | 0.575 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.282 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.366 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.624 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.341 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.319 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.446 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.482 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.485 |
TRG_DiLeu_BaEn_1 | 267 | 272 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5T0 | Leptomonas seymouri | 76% | 100% |
A0A0S4INP7 | Bodo saltans | 40% | 88% |
A0A1X0NW56 | Trypanosomatidae | 52% | 98% |
A0A3R7RG23 | Trypanosoma rangeli | 52% | 99% |
A0A3S7WW32 | Leishmania donovani | 89% | 100% |
A4HYY6 | Leishmania infantum | 92% | 100% |
C9ZIJ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 96% |
E9AUT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QCQ1 | Leishmania major | 87% | 100% |
V5BDU9 | Trypanosoma cruzi | 53% | 100% |