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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B0W8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.503 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.495 |
DEG_SCF_FBW7_1 | 20 | 27 | PF00400 | 0.233 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.504 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.395 |
DEG_SPOP_SBC_1 | 241 | 245 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.698 |
DOC_CYCLIN_RxL_1 | 403 | 414 | PF00134 | 0.513 |
DOC_CYCLIN_RxL_1 | 84 | 92 | PF00134 | 0.395 |
DOC_MAPK_DCC_7 | 163 | 171 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 370 | 379 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 163 | 171 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 372 | 381 | PF00069 | 0.479 |
DOC_MAPK_RevD_3 | 249 | 265 | PF00069 | 0.514 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.649 |
DOC_PP4_FxxP_1 | 224 | 227 | PF00568 | 0.497 |
DOC_SPAK_OSR1_1 | 163 | 167 | PF12202 | 0.757 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.611 |
DOC_USP7_MATH_2 | 333 | 339 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.406 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 397 | 404 | PF00244 | 0.584 |
LIG_Actin_WH2_2 | 381 | 398 | PF00022 | 0.648 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.503 |
LIG_deltaCOP1_diTrp_1 | 158 | 164 | PF00928 | 0.497 |
LIG_eIF4E_1 | 84 | 90 | PF01652 | 0.395 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.736 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.411 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.618 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.568 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.709 |
LIG_Integrin_RGD_1 | 361 | 363 | PF01839 | 0.636 |
LIG_LIR_Apic_2 | 258 | 263 | PF02991 | 0.585 |
LIG_LIR_Apic_2 | 269 | 275 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 158 | 169 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 65 | 73 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 78 | 86 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.457 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.474 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.708 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.406 |
LIG_SH3_1 | 272 | 278 | PF00018 | 0.697 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.708 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.577 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.730 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.233 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.529 |
MOD_CDC14_SPxK_1 | 139 | 142 | PF00782 | 0.646 |
MOD_CDK_SPK_2 | 20 | 25 | PF00069 | 0.233 |
MOD_CDK_SPK_2 | 301 | 306 | PF00069 | 0.706 |
MOD_CDK_SPK_2 | 329 | 334 | PF00069 | 0.612 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.655 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.708 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.669 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.589 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.595 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.650 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.602 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.641 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.721 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.461 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.608 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.647 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.642 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.558 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.447 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.668 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.628 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.563 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.631 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.728 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.357 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.694 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.449 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.558 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.714 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.659 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.636 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.233 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.551 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.627 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.570 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.651 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.544 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.695 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.536 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.552 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.757 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.624 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.513 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.529 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.665 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.690 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.673 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.506 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.503 |
MOD_PK_1 | 361 | 367 | PF00069 | 0.584 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.521 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.484 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.653 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.395 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.767 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.657 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.697 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.536 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.503 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.679 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.659 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.664 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.599 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.622 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.610 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.233 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.661 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.578 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.705 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.770 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.406 |
TRG_DiLeu_BaEn_2 | 1 | 7 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_4 | 390 | 396 | PF01217 | 0.655 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.698 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 87 | 92 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IML8 | Leptomonas seymouri | 33% | 93% |
A0A3Q8IEA2 | Leishmania donovani | 79% | 97% |
A4HID0 | Leishmania braziliensis | 55% | 100% |
A4I5M3 | Leishmania infantum | 79% | 97% |