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: E9AIM0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.611 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.589 |
CLV_Separin_Metazoa | 119 | 123 | PF03568 | 0.574 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.449 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.691 |
DOC_MAPK_gen_1 | 159 | 168 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 269 | 278 | PF00069 | 0.382 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.526 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.457 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 5 | 12 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 80 | 88 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 58 | 75 | PF00022 | 0.574 |
LIG_BIR_III_2 | 74 | 78 | PF00653 | 0.434 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.510 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.561 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.464 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.509 |
LIG_Integrin_isoDGR_2 | 267 | 269 | PF01839 | 0.515 |
LIG_LIR_Apic_2 | 188 | 194 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.424 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.372 |
LIG_RPA_C_Fungi | 296 | 308 | PF08784 | 0.583 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.424 |
LIG_SH2_GRB2like | 283 | 286 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 272 | 275 | PF00017 | 0.353 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.484 |
LIG_SH2_SRC | 283 | 286 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 105 | 108 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.353 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.594 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.555 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 183 | 189 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 286 | 291 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 274 | 282 | PF11976 | 0.402 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.487 |
LIG_UBA3_1 | 168 | 174 | PF00899 | 0.376 |
LIG_WW_2 | 193 | 196 | PF00397 | 0.462 |
MOD_CDK_SPxxK_3 | 73 | 80 | PF00069 | 0.647 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.672 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.734 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.535 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.524 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.468 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.484 |
MOD_GlcNHglycan | 137 | 141 | PF01048 | 0.580 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.790 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.470 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.566 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.609 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.555 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.511 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.573 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.591 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.391 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.775 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.673 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.565 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.593 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.406 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.754 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.592 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.388 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.389 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.373 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.514 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.506 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.627 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.563 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.497 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.335 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.588 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.504 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.703 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.432 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.392 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.391 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.628 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.560 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.550 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.525 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.636 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.399 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.610 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.353 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0J0 | Leptomonas seymouri | 67% | 100% |
A0A1X0NWJ0 | Trypanosomatidae | 50% | 100% |
A0A3Q8IKS5 | Leishmania donovani | 84% | 100% |
A0A422NTQ6 | Trypanosoma rangeli | 48% | 100% |
A4HZ01 | Leishmania infantum | 83% | 100% |
C9ZIM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AUV3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QCN0 | Leishmania major | 84% | 100% |
V5B8D6 | Trypanosoma cruzi | 49% | 100% |