A protein with very uncertain structure. However, it does not appear to be transmembrane.
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: E9B4F5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.432 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.759 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 431 | 435 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.644 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.483 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.673 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.704 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.697 |
DOC_CYCLIN_RxL_1 | 453 | 464 | PF00134 | 0.442 |
DOC_MAPK_MEF2A_6 | 179 | 187 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 118 | 125 | PF00149 | 0.653 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.673 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.704 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.681 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.676 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 53 | 63 | PF00244 | 0.703 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.730 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.580 |
LIG_deltaCOP1_diTrp_1 | 221 | 226 | PF00928 | 0.647 |
LIG_deltaCOP1_diTrp_1 | 412 | 419 | PF00928 | 0.516 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.392 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.740 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.698 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.337 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.312 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.677 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.586 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.509 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.464 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.649 |
LIG_LIR_Apic_2 | 482 | 488 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 57 | 63 | PF02991 | 0.729 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 238 | 246 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 341 | 349 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 412 | 422 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 92 | 101 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.641 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.475 |
LIG_PCNA_PIPBox_1 | 243 | 252 | PF02747 | 0.441 |
LIG_Pex14_1 | 222 | 226 | PF04695 | 0.648 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.344 |
LIG_SH2_SRC | 485 | 488 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.358 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.704 |
LIG_SH3_4 | 292 | 299 | PF00018 | 0.486 |
LIG_SUMO_SIM_par_1 | 183 | 188 | PF11976 | 0.583 |
LIG_SxIP_EBH_1 | 442 | 456 | PF03271 | 0.543 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.621 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.442 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.486 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.504 |
LIG_UBA3_1 | 183 | 191 | PF00899 | 0.625 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.731 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.493 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.423 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.696 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.605 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.599 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.682 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.562 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.452 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.546 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.476 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.706 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.717 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.691 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.723 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.448 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.748 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.625 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.436 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.741 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.650 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.403 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.372 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.629 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.682 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.760 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.716 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.416 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.602 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.727 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.676 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.757 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.682 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.483 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.728 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.714 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.487 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.539 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.744 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.506 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.673 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.344 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.344 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.278 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.748 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.685 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.480 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.684 |
MOD_SUMO_for_1 | 30 | 33 | PF00179 | 0.698 |
MOD_SUMO_rev_2 | 22 | 30 | PF00179 | 0.712 |
MOD_SUMO_rev_2 | 365 | 372 | PF00179 | 0.565 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.594 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 430 | 435 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 53 | 58 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE42 | Leptomonas seymouri | 66% | 100% |
A0A0S4JAR7 | Bodo saltans | 39% | 87% |
A0A1X0NS34 | Trypanosomatidae | 49% | 92% |
A0A3R7N841 | Trypanosoma rangeli | 50% | 95% |
A0A3S5H7V5 | Leishmania donovani | 92% | 100% |
A4HM23 | Leishmania braziliensis | 81% | 99% |
A4I9F7 | Leishmania infantum | 92% | 100% |
C9ZJT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 93% |
Q4Q3M0 | Leishmania major | 91% | 100% |
V5B2X5 | Trypanosoma cruzi | 45% | 100% |