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: A0A3S5H7B8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.482 |
DEG_SCF_FBW7_1 | 131 | 136 | PF00400 | 0.605 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.627 |
DOC_ANK_TNKS_1 | 203 | 210 | PF00023 | 0.665 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.571 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.586 |
DOC_CYCLIN_RxL_1 | 182 | 194 | PF00134 | 0.593 |
DOC_CYCLIN_RxL_1 | 278 | 289 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 332 | 342 | PF00134 | 0.474 |
DOC_PP1_RVXF_1 | 279 | 286 | PF00149 | 0.598 |
DOC_PP1_RVXF_1 | 332 | 339 | PF00149 | 0.454 |
DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.465 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.605 |
DOC_USP7_MATH_2 | 198 | 204 | PF00917 | 0.677 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 335 | 343 | PF00244 | 0.558 |
LIG_APCC_ABBA_1 | 285 | 290 | PF00400 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.552 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.437 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.528 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.553 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.437 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.523 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.406 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.644 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.632 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.546 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.441 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.404 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.572 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.392 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.513 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.535 |
LIG_SH2_PTP2 | 299 | 302 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.460 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.598 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.537 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.776 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.525 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.588 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.528 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.669 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.618 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.583 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.502 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.648 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.676 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.673 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.559 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.404 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.607 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.625 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.527 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.465 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.559 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.402 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.570 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.661 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.698 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.727 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.668 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.640 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.650 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.500 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.575 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.475 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.692 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.643 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.656 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.573 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.668 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.516 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.633 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.384 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.689 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.402 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.609 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.671 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.525 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.618 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.611 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.661 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.607 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.397 |
MOD_Plk_2-3 | 271 | 277 | PF00069 | 0.608 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.598 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.677 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.590 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.497 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.376 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.444 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.576 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.607 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.585 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.595 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.458 |
MOD_SUMO_rev_2 | 192 | 198 | PF00179 | 0.662 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE95 | Leptomonas seymouri | 47% | 88% |
A4HCS4 | Leishmania braziliensis | 74% | 100% |
A4I098 | Leishmania infantum | 99% | 100% |
E9AW63 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QBB5 | Leishmania major | 88% | 100% |