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: Q4QHD2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.688 |
DEG_APCC_DBOX_1 | 310 | 318 | PF00400 | 0.519 |
DEG_APCC_DBOX_1 | 360 | 368 | PF00400 | 0.445 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.649 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.654 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.567 |
DOC_CKS1_1 | 70 | 75 | PF01111 | 0.577 |
DOC_CYCLIN_RxL_1 | 94 | 104 | PF00134 | 0.687 |
DOC_MAPK_gen_1 | 309 | 319 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 147 | 153 | PF00149 | 0.648 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.567 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.551 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.441 |
LIG_14-3-3_CterR_2 | 396 | 400 | PF00244 | 0.703 |
LIG_Actin_WH2_2 | 77 | 92 | PF00022 | 0.683 |
LIG_APCC_ABBA_1 | 278 | 283 | PF00400 | 0.410 |
LIG_APCC_ABBAyCdc20_2 | 277 | 283 | PF00400 | 0.409 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_2 | 258 | 264 | PF00533 | 0.539 |
LIG_CSL_BTD_1 | 57 | 60 | PF09270 | 0.671 |
LIG_CtBP_PxDLS_1 | 255 | 261 | PF00389 | 0.564 |
LIG_CtBP_PxDLS_1 | 98 | 102 | PF00389 | 0.578 |
LIG_deltaCOP1_diTrp_1 | 55 | 65 | PF00928 | 0.609 |
LIG_EVH1_2 | 129 | 133 | PF00568 | 0.557 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.412 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.693 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.614 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.572 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.624 |
LIG_LIR_Apic_2 | 166 | 171 | PF02991 | 0.550 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.543 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.620 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.610 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.451 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.591 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.509 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.582 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.580 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.693 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.634 |
LIG_TRAF2_1 | 372 | 375 | PF00917 | 0.534 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.758 |
LIG_WRC_WIRS_1 | 328 | 333 | PF05994 | 0.530 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.635 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.637 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.496 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.694 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.572 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.544 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.659 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.671 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.483 |
MOD_LATS_1 | 325 | 331 | PF00433 | 0.391 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.502 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.613 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.617 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.654 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.452 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.484 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.581 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.420 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.559 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.709 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.446 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.419 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.577 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.635 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.613 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 305 | 308 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 141 | 151 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 159 | 165 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 215 | 223 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 82 | 92 | PF00179 | 0.570 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_3 | 122 | 128 | PF01217 | 0.700 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU6 | Leptomonas seymouri | 88% | 79% |
A0A0S4JP89 | Bodo saltans | 62% | 87% |
A0A1X0NQD3 | Trypanosomatidae | 78% | 83% |
A0A3S7WR96 | Leishmania donovani | 99% | 100% |
A4H670 | Leishmania braziliensis | 96% | 100% |
A4HUJ4 | Leishmania infantum | 99% | 100% |
C9ZVL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 86% |
E9AN92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
V5B434 | Trypanosoma cruzi | 78% | 81% |