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: A4H3X3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.682 |
CLV_MEL_PAP_1 | 29 | 35 | PF00089 | 0.654 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.702 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.658 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.673 |
DEG_APCC_KENBOX_2 | 325 | 329 | PF00400 | 0.541 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.709 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.735 |
DOC_CDC14_PxL_1 | 120 | 128 | PF14671 | 0.591 |
DOC_CKS1_1 | 243 | 248 | PF01111 | 0.685 |
DOC_CKS1_1 | 312 | 317 | PF01111 | 0.553 |
DOC_CYCLIN_RxL_1 | 154 | 163 | PF00134 | 0.372 |
DOC_CYCLIN_RxL_1 | 307 | 317 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 312 | 318 | PF00134 | 0.652 |
DOC_MAPK_gen_1 | 332 | 338 | PF00069 | 0.526 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.798 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.547 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.524 |
LIG_BIR_III_2 | 294 | 298 | PF00653 | 0.623 |
LIG_CtBP_PxDLS_1 | 246 | 250 | PF00389 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 136 | 142 | PF00928 | 0.506 |
LIG_EH_1 | 35 | 39 | PF12763 | 0.578 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.586 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.524 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.676 |
LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.536 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.718 |
LIG_SH2_NCK_1 | 293 | 297 | PF00017 | 0.718 |
LIG_SH3_1 | 48 | 54 | PF00018 | 0.814 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.542 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.768 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.779 |
LIG_Sin3_3 | 353 | 360 | PF02671 | 0.759 |
LIG_Sin3_3 | 8 | 15 | PF02671 | 0.535 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 214 | 223 | PF11976 | 0.655 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.564 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.644 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.546 |
MOD_CDK_SPK_2 | 66 | 71 | PF00069 | 0.580 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.583 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.621 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.823 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.563 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.506 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.509 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.731 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.629 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.594 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.642 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.706 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.607 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.750 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.604 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.669 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.360 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.787 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.503 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.790 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.593 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.521 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.581 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.612 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.712 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.549 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.664 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.554 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.429 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.670 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.557 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.442 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.529 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.521 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.582 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.608 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.716 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.668 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.676 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.577 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.580 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.546 |
MOD_SUMO_rev_2 | 173 | 183 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 359 | 369 | PF00179 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 121 | 126 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.717 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0N8 | Leptomonas seymouri | 40% | 100% |
A0A3S7WNR0 | Leishmania donovani | 63% | 100% |
A4HS48 | Leishmania infantum | 63% | 100% |
E9AK35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 96% |
O97202 | Leishmania major | 62% | 100% |