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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H9D8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.753 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.459 |
DEG_APCC_KENBOX_2 | 123 | 127 | PF00400 | 0.450 |
DEG_SCF_FBW7_1 | 48 | 54 | PF00400 | 0.465 |
DEG_SIAH_1 | 401 | 409 | PF03145 | 0.461 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.411 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.467 |
DOC_PP1_RVXF_1 | 128 | 134 | PF00149 | 0.469 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 211 | 221 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 382 | 391 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 449 | 454 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.564 |
LIG_deltaCOP1_diTrp_1 | 252 | 261 | PF00928 | 0.266 |
LIG_deltaCOP1_diTrp_1 | 305 | 315 | PF00928 | 0.411 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.383 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.575 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.662 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.411 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.257 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 224 | 229 | PF02991 | 0.285 |
LIG_LIR_Apic_2 | 429 | 434 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.555 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.281 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.331 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.461 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.294 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.431 |
LIG_SH3_1 | 241 | 247 | PF00018 | 0.331 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.459 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.268 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.491 |
LIG_SUMO_SIM_par_1 | 246 | 253 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.441 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.443 |
LIG_TYR_ITIM | 421 | 426 | PF00017 | 0.292 |
MOD_CDC14_SPxK_1 | 11 | 14 | PF00782 | 0.513 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.462 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.511 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.407 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.591 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.325 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.360 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.580 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.726 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.479 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.694 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.461 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.411 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.257 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.602 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.392 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.684 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.341 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.360 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.360 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.547 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.651 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.644 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.451 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.510 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.348 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.145 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.479 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.698 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.575 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.619 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.539 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.669 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.448 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.517 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.484 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.520 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.679 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.679 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.404 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.696 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.585 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.560 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.703 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.467 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.494 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.266 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.459 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.578 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.543 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.411 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.618 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.511 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.252 |
TRG_NES_CRM1_1 | 337 | 349 | PF08389 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 120 | 125 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 81 | 86 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P400 | Leptomonas seymouri | 58% | 100% |
A0A1X0P6R6 | Trypanosomatidae | 43% | 100% |
A0A3Q8IAW5 | Leishmania donovani | 79% | 100% |
A0A422NWL4 | Trypanosoma rangeli | 41% | 100% |
A4HXQ9 | Leishmania infantum | 79% | 100% |
B6DTF3 | Bodo saltans | 32% | 100% |
D0A041 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9ARH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QE08 | Leishmania major | 79% | 100% |
V5DN00 | Trypanosoma cruzi | 40% | 100% |