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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H9F8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.457 |
CLV_PCSK_FUR_1 | 417 | 421 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.674 |
CLV_PCSK_PC7_1 | 71 | 77 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.361 |
CLV_Separin_Metazoa | 294 | 298 | PF03568 | 0.479 |
DEG_APCC_DBOX_1 | 289 | 297 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 171 | 175 | PF00917 | 0.455 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.460 |
DOC_CKS1_1 | 356 | 361 | PF01111 | 0.509 |
DOC_MAPK_gen_1 | 107 | 114 | PF00069 | 0.616 |
DOC_MAPK_RevD_3 | 403 | 418 | PF00069 | 0.283 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.584 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.712 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 107 | 114 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.497 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.228 |
LIG_deltaCOP1_diTrp_1 | 139 | 147 | PF00928 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 250 | 257 | PF00928 | 0.443 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.483 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.571 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.511 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.437 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.628 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.522 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.592 |
LIG_LIR_Apic_2 | 220 | 225 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 366 | 374 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 399 | 408 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.463 |
LIG_MLH1_MIPbox_1 | 219 | 223 | PF16413 | 0.228 |
LIG_PCNA_PIPBox_1 | 22 | 31 | PF02747 | 0.489 |
LIG_PCNA_yPIPBox_3 | 15 | 29 | PF02747 | 0.493 |
LIG_Pex14_1 | 253 | 257 | PF04695 | 0.475 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.359 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.482 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.606 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.476 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.605 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.476 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 404 | 410 | PF11976 | 0.488 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.467 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.369 |
LIG_UBA3_1 | 370 | 379 | PF00899 | 0.368 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.672 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.532 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.460 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.654 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.666 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.692 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.489 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.233 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.593 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.696 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.532 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.602 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.288 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.627 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.628 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.506 |
MOD_GlcNHglycan | 164 | 168 | PF01048 | 0.463 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.578 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.364 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.441 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.300 |
MOD_GlcNHglycan | 245 | 249 | PF01048 | 0.632 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.461 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.572 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.457 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.681 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.714 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.690 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.558 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.361 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.588 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.498 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.595 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.656 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.682 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.538 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.508 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.666 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.580 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.578 |
MOD_N-GLC_2 | 277 | 279 | PF02516 | 0.314 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.495 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.478 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.515 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.421 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.486 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.703 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.468 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.670 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.533 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.328 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.617 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.701 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.492 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.488 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.531 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.520 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.657 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.383 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.468 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.636 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.461 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.468 |
TRG_NLS_MonoCore_2 | 415 | 420 | PF00514 | 0.318 |
TRG_NLS_MonoExtC_3 | 415 | 420 | PF00514 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5D0 | Leptomonas seymouri | 53% | 98% |
A0A1X0P6Z6 | Trypanosomatidae | 39% | 100% |
A0A3Q8IB26 | Leishmania donovani | 78% | 100% |
A0A422NJ49 | Trypanosoma rangeli | 37% | 100% |
A4HXS5 | Leishmania infantum | 78% | 100% |
D0A057 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9ARI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QDZ2 | Leishmania major | 78% | 100% |
V5BRN6 | Trypanosoma cruzi | 33% | 100% |