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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QHF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.467 |
CLV_PCSK_FUR_1 | 115 | 119 | PF00082 | 0.514 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.593 |
CLV_PCSK_FUR_1 | 79 | 83 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 113 | 119 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.515 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.440 |
DEG_Kelch_Keap1_1 | 207 | 212 | PF01344 | 0.630 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.661 |
DOC_CYCLIN_RxL_1 | 178 | 186 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 123 | 129 | PF00134 | 0.552 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 377 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 115 | 125 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.614 |
DOC_MAPK_MEF2A_6 | 118 | 127 | PF00069 | 0.458 |
DOC_MAPK_RevD_3 | 65 | 79 | PF00069 | 0.548 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.532 |
DOC_PP1_RVXF_1 | 333 | 339 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.390 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.586 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.747 |
LIG_14-3-3_CanoR_1 | 170 | 180 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.647 |
LIG_APCC_ABBA_1 | 361 | 366 | PF00400 | 0.517 |
LIG_CaM_IQ_9 | 185 | 200 | PF13499 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 366 | 372 | PF00928 | 0.518 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.487 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.498 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.570 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.638 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.508 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.484 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.571 |
LIG_GBD_Chelix_1 | 341 | 349 | PF00786 | 0.515 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 337 | 345 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 346 | 355 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.655 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.590 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.515 |
LIG_PTB_Apo_2 | 307 | 314 | PF02174 | 0.556 |
LIG_PTB_Phospho_1 | 307 | 313 | PF10480 | 0.548 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.465 |
LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 63 | 70 | PF11976 | 0.496 |
LIG_TRFH_1 | 372 | 376 | PF08558 | 0.557 |
LIG_TYR_ITIM | 345 | 350 | PF00017 | 0.479 |
LIG_UBA3_1 | 162 | 171 | PF00899 | 0.515 |
LIG_UBA3_1 | 184 | 193 | PF00899 | 0.537 |
MOD_CDK_SPxxK_3 | 251 | 258 | PF00069 | 0.585 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.492 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.565 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.481 |
MOD_Cter_Amidation | 33 | 36 | PF01082 | 0.479 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.581 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.705 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.602 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.547 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.474 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.662 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.480 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.482 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.429 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.400 |
MOD_PK_1 | 121 | 127 | PF00069 | 0.476 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.478 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.611 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.559 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.522 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.476 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.493 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.588 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.747 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.608 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 258 | 263 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X7 | Leptomonas seymouri | 35% | 96% |
A0A3S7WR94 | Leishmania donovani | 92% | 100% |
A4H657 | Leishmania braziliensis | 75% | 100% |
A4HUH7 | Leishmania infantum | 93% | 100% |
E9AN75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |