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: A4HQ15
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 168 | 174 | PF00089 | 0.440 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.441 |
CLV_PCSK_FUR_1 | 66 | 70 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.351 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.555 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.520 |
DOC_CDC14_PxL_1 | 231 | 239 | PF14671 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 13 | PF00134 | 0.516 |
DOC_MAPK_FxFP_2 | 318 | 321 | PF00069 | 0.474 |
DOC_PP1_RVXF_1 | 209 | 216 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.614 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.383 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.378 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.615 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 270 | 288 | PF00022 | 0.370 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.520 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.468 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.417 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.482 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.595 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.543 |
LIG_GBD_Chelix_1 | 300 | 308 | PF00786 | 0.425 |
LIG_IBAR_NPY_1 | 27 | 29 | PF08397 | 0.556 |
LIG_LIR_Apic_2 | 174 | 180 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 222 | 228 | PF02991 | 0.485 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.552 |
LIG_PCNA_PIPBox_1 | 92 | 101 | PF02747 | 0.557 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.443 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.401 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.381 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.705 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.381 |
LIG_SH2_SRC | 48 | 51 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.500 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.430 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.473 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.436 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.375 |
LIG_WRC_WIRS_1 | 181 | 186 | PF05994 | 0.498 |
LIG_WW_3 | 11 | 15 | PF00397 | 0.515 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.655 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.723 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.724 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.523 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.416 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.584 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.510 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.497 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.450 |
MOD_Cter_Amidation | 66 | 69 | PF01082 | 0.546 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.611 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.611 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.563 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.429 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.474 |
MOD_GlcNHglycan | 256 | 260 | PF01048 | 0.358 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.527 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.622 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.582 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.418 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.507 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.489 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.545 |
MOD_NEK2_2 | 42 | 47 | PF00069 | 0.411 |
MOD_PK_1 | 164 | 170 | PF00069 | 0.387 |
MOD_PKA_1 | 68 | 74 | PF00069 | 0.544 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.544 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.507 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.475 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.425 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.510 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.509 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.477 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.591 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 243 | 250 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 269 | 274 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.712 |
TRG_NES_CRM1_1 | 299 | 312 | PF08389 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBG8 | Leptomonas seymouri | 59% | 98% |
A0A3Q8IJQ3 | Leishmania donovani | 77% | 99% |
A4IDS1 | Leishmania infantum | 77% | 99% |
E9ATT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 98% |
Q4Q0R4 | Leishmania major | 76% | 100% |