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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9ASG9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.471 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.522 |
DOC_MAPK_gen_1 | 200 | 207 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.338 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.455 |
DOC_PP2B_PxIxI_1 | 328 | 334 | PF00149 | 0.582 |
DOC_PP4_FxxP_1 | 268 | 271 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.440 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 315 | 324 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 125 | 143 | PF00022 | 0.391 |
LIG_Actin_WH2_2 | 376 | 394 | PF00022 | 0.472 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.426 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.423 |
LIG_Clathr_ClatBox_1 | 380 | 384 | PF01394 | 0.483 |
LIG_EH1_1 | 206 | 214 | PF00400 | 0.388 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.437 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.403 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.473 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.636 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.459 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.547 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.422 |
LIG_GBD_Chelix_1 | 10 | 18 | PF00786 | 0.445 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 244 | 255 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.278 |
LIG_MYND_1 | 55 | 59 | PF01753 | 0.755 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.406 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.468 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.359 |
LIG_Rb_LxCxE_1 | 249 | 267 | PF01857 | 0.433 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.580 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.484 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.465 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.468 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.500 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.611 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 376 | 382 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 379 | 384 | PF11976 | 0.481 |
LIG_UBA3_1 | 356 | 360 | PF00899 | 0.481 |
LIG_WRC_WIRS_1 | 265 | 270 | PF05994 | 0.575 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.567 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.719 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.440 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.513 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.474 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.766 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.488 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.463 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.421 |
MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.499 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.673 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.419 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.376 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.668 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.564 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.356 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.483 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.633 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.579 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.691 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.503 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.514 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.452 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.436 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.503 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.516 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.610 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.491 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.711 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.743 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.514 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.391 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.467 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.456 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.542 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.533 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.508 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.620 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.567 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.484 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.407 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.527 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.610 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.594 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.385 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.659 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.308 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.426 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.574 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.583 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 4 | 7 | PF00179 | 0.438 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 107 | 116 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 355 | 361 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 384 | 394 | PF00179 | 0.392 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.446 |
TRG_DiLeu_LyEn_5 | 29 | 34 | PF01217 | 0.305 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.412 |
TRG_NES_CRM1_1 | 28 | 43 | PF08389 | 0.434 |
TRG_NLS_MonoExtN_4 | 32 | 39 | PF00514 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JPJ4 | Bodo saltans | 34% | 86% |
A0A1X0P9M8 | Trypanosomatidae | 36% | 100% |
A0A3Q8IFS3 | Leishmania donovani | 89% | 100% |
A0A422P297 | Trypanosoma rangeli | 37% | 99% |
A4HNR0 | Leishmania braziliensis | 72% | 100% |
A4ICT5 | Leishmania infantum | 89% | 100% |
D0A2L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q226 | Leishmania major | 90% | 100% |