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: 15 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H5E9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.603 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.524 |
CLV_PCSK_FUR_1 | 134 | 138 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.357 |
CLV_Separin_Metazoa | 26 | 30 | PF03568 | 0.418 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.442 |
DEG_SCF_FBW7_2 | 107 | 114 | PF00400 | 0.470 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.474 |
DOC_MAPK_gen_1 | 18 | 25 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 269 | 276 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 269 | 276 | PF00069 | 0.511 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.580 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 41 | 50 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 65 | 74 | PF00244 | 0.544 |
LIG_Actin_WH2_2 | 70 | 87 | PF00022 | 0.493 |
LIG_CSL_BTD_1 | 262 | 265 | PF09270 | 0.500 |
LIG_EVH1_1 | 3 | 7 | PF00568 | 0.613 |
LIG_EVH1_2 | 4 | 8 | PF00568 | 0.617 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.560 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.473 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.587 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.434 |
LIG_LIR_Gen_1 | 99 | 108 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.446 |
LIG_NRBOX | 205 | 211 | PF00104 | 0.429 |
LIG_PCNA_yPIPBox_3 | 229 | 241 | PF02747 | 0.427 |
LIG_Pex14_1 | 152 | 156 | PF04695 | 0.418 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.467 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.425 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 172 | 176 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.538 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.628 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.479 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 204 | 211 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 204 | 211 | PF11976 | 0.427 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.595 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.508 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.685 |
LIG_TYR_ITIM | 170 | 175 | PF00017 | 0.523 |
LIG_UBA3_1 | 222 | 229 | PF00899 | 0.434 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.654 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.507 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.477 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.526 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.476 |
MOD_GlcNHglycan | 256 | 260 | PF01048 | 0.605 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.559 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.560 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.498 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.551 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.565 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.441 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.522 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.606 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.411 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.498 |
MOD_PKA_1 | 18 | 24 | PF00069 | 0.502 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.530 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.430 |
MOD_PKB_1 | 169 | 177 | PF00069 | 0.504 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.445 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.416 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.471 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.512 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 112 | 118 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 153 | 159 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 331 | 341 | PF00179 | 0.693 |
TRG_DiLeu_BaEn_1 | 205 | 210 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 267 | 272 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_4 | 267 | 273 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 312 | 317 | PF01217 | 0.485 |
TRG_DiLeu_LyEn_5 | 267 | 272 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.694 |
TRG_ER_diLys_1 | 338 | 342 | PF00400 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 162 | 167 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5W5 | Leptomonas seymouri | 84% | 94% |
A0A0S4IPK0 | Bodo saltans | 66% | 93% |
A0A1X0NPG5 | Trypanosomatidae | 75% | 92% |
A0A3S5H687 | Leishmania donovani | 93% | 94% |
A0A422NFX7 | Trypanosoma rangeli | 69% | 92% |
A4HTP3 | Leishmania infantum | 93% | 94% |
C9ZPE5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 92% |
E9AMI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 94% |
Q4QI59 | Leishmania major | 93% | 100% |
V5DAE9 | Trypanosoma cruzi | 72% | 92% |