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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QD09
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.467 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.407 |
DOC_ANK_TNKS_1 | 157 | 164 | PF00023 | 0.566 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.654 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 328 | 334 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.717 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.517 |
DOC_PIKK_1 | 253 | 261 | PF02985 | 0.510 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.383 |
DOC_PP1_RVXF_1 | 63 | 70 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.538 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 377 | 380 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 363 | 372 | PF00244 | 0.673 |
LIG_Actin_WH2_2 | 344 | 362 | PF00022 | 0.530 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.645 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.566 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.529 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.549 |
LIG_LIR_LC3C_4 | 132 | 137 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.543 |
LIG_MYND_1 | 376 | 380 | PF01753 | 0.674 |
LIG_PAM2_1 | 145 | 157 | PF00658 | 0.426 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 352 | 355 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.525 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.575 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.443 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.534 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.630 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.580 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.450 |
LIG_SUMO_SIM_anti_2 | 240 | 248 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 286 | 291 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.608 |
LIG_TRAF2_1 | 186 | 189 | PF00917 | 0.672 |
MOD_CDK_SPK_2 | 384 | 389 | PF00069 | 0.631 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.746 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.647 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.625 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.330 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.476 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.633 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.541 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.516 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.562 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.594 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.568 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.630 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.666 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.607 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.346 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.479 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.479 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.343 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.522 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.467 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.466 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.346 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.582 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.445 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.371 |
MOD_PKA_1 | 44 | 50 | PF00069 | 0.603 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.664 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.494 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.566 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.348 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.497 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.489 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.632 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.688 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.444 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.612 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.630 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 248 | 258 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 260 | 268 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 333 | 342 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.467 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.649 |
TRG_NLS_MonoCore_2 | 208 | 213 | PF00514 | 0.622 |
TRG_NLS_MonoExtC_3 | 208 | 213 | PF00514 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWV5 | Leptomonas seymouri | 59% | 95% |
A0A3S7WVR4 | Leishmania donovani | 92% | 100% |
A4HYS0 | Leishmania infantum | 92% | 100% |
C9ZIA4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AI90 | Leishmania braziliensis | 77% | 100% |
E9AUH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BVI5 | Trypanosoma cruzi | 30% | 100% |