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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QJH7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.685 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.468 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.445 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.535 |
DOC_MAPK_MEF2A_6 | 178 | 187 | PF00069 | 0.600 |
DOC_SPAK_OSR1_1 | 246 | 250 | PF12202 | 0.503 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.649 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.438 |
LIG_CtBP_PxDLS_1 | 184 | 188 | PF00389 | 0.477 |
LIG_CtBP_PxDLS_1 | 78 | 83 | PF00389 | 0.469 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.410 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.526 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.391 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.570 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.556 |
LIG_LIR_Gen_1 | 317 | 327 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.522 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.397 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.562 |
LIG_SUMO_SIM_anti_2 | 298 | 303 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 297 | 303 | PF11976 | 0.423 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.572 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.433 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.445 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.688 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.497 |
LIG_TYR_ITIM | 152 | 157 | PF00017 | 0.409 |
MOD_CDK_SPxK_1 | 282 | 288 | PF00069 | 0.543 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.649 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.367 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.460 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.672 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.608 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.493 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.541 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.688 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.463 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.447 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.587 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.583 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.779 |
MOD_GlcNHglycan | 373 | 379 | PF01048 | 0.747 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.421 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.449 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.565 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.620 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.461 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.654 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.480 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.455 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.567 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.427 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.526 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.544 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.645 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.544 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.521 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.387 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.453 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.542 |
TRG_DiLeu_BaEn_1 | 80 | 85 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_2 | 315 | 321 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_3 | 316 | 322 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.487 |
TRG_NLS_MonoExtN_4 | 222 | 228 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHU8 | Leptomonas seymouri | 45% | 94% |
A0A3S7WP15 | Leishmania donovani | 88% | 100% |
A4H470 | Leishmania braziliensis | 72% | 100% |
A4HSE5 | Leishmania infantum | 88% | 100% |
E9AKD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |