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 |
Related structures:
AlphaFold database: E9AH18
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.449 |
CLV_Separin_Metazoa | 272 | 276 | PF03568 | 0.516 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.577 |
DEG_SCF_FBW7_1 | 85 | 92 | PF00400 | 0.598 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.614 |
DOC_CYCLIN_RxL_1 | 164 | 174 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.585 |
DOC_MAPK_gen_1 | 263 | 273 | PF00069 | 0.520 |
DOC_MAPK_RevD_3 | 61 | 77 | PF00069 | 0.486 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.536 |
DOC_PP4_MxPP_1 | 82 | 85 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.571 |
LIG_14-3-3_CanoR_1 | 106 | 111 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 209 | 219 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.259 |
LIG_Actin_WH2_2 | 218 | 236 | PF00022 | 0.292 |
LIG_APCC_ABBA_1 | 301 | 306 | PF00400 | 0.506 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.503 |
LIG_EH_1 | 155 | 159 | PF12763 | 0.447 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.499 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.580 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.504 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.597 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.476 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 306 | 310 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.480 |
LIG_MAD2 | 78 | 86 | PF02301 | 0.377 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.489 |
LIG_SH2_SRC | 175 | 178 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.502 |
LIG_SH2_STAT3 | 323 | 326 | PF00017 | 0.517 |
LIG_SH2_STAT3 | 47 | 50 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.512 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.559 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.577 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.514 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.573 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.423 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.450 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.600 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.467 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.503 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.488 |
MOD_GlcNHglycan | 97 | 101 | PF01048 | 0.538 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.459 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.490 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.463 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.503 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.532 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.401 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.414 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.422 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.438 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.497 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.468 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.373 |
MOD_OFUCOSY | 87 | 93 | PF10250 | 0.484 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.427 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.414 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.462 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.532 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.500 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.523 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.589 |
MOD_PKB_1 | 104 | 112 | PF00069 | 0.520 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.545 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.552 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.468 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.536 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.561 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.609 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.624 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.571 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 273 | 278 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 291 | 306 | PF08389 | 0.476 |
TRG_NLS_MonoCore_2 | 74 | 79 | PF00514 | 0.367 |
TRG_NLS_MonoExtN_4 | 72 | 79 | PF00514 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC82 | Leptomonas seymouri | 52% | 100% |
A0A1X0NWL6 | Trypanosomatidae | 28% | 100% |
A0A3S7WY36 | Leishmania donovani | 98% | 100% |
A0A422NJF2 | Trypanosoma rangeli | 29% | 99% |
A4HD40 | Leishmania braziliensis | 76% | 100% |
C9ZNR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AWI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QAY2 | Leishmania major | 93% | 100% |
V5BFT2 | Trypanosoma cruzi | 28% | 95% |