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: Q4QG68
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.646 |
CLV_PCSK_FUR_1 | 155 | 159 | PF00082 | 0.725 |
CLV_PCSK_FUR_1 | 411 | 415 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.827 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.827 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 157 | 163 | PF00082 | 0.757 |
CLV_PCSK_PC7_1 | 409 | 415 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.826 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.464 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.466 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.665 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.537 |
DOC_MAPK_DCC_7 | 16 | 25 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 32 | 39 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 60 | 69 | PF00069 | 0.532 |
DOC_PP4_FxxP_1 | 228 | 231 | PF00568 | 0.734 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.489 |
DOC_USP7_MATH_2 | 125 | 131 | PF00917 | 0.629 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.677 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.402 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.406 |
LIG_Actin_WH2_2 | 62 | 77 | PF00022 | 0.519 |
LIG_AP2alpha_2 | 200 | 202 | PF02296 | 0.693 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.796 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.452 |
LIG_CSL_BTD_1 | 239 | 242 | PF09270 | 0.683 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.742 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.552 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.421 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.723 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.453 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.671 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.630 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.559 |
LIG_Integrin_isoDGR_2 | 343 | 345 | PF01839 | 0.758 |
LIG_LIR_Apic_2 | 136 | 141 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 34 | 43 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.394 |
LIG_MYND_1 | 20 | 24 | PF01753 | 0.453 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.456 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.437 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.443 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.657 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.682 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.693 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.780 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.585 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.737 |
LIG_UBA3_1 | 418 | 423 | PF00899 | 0.432 |
MOD_CDK_SPxxK_3 | 148 | 155 | PF00069 | 0.683 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.532 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.427 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.699 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.477 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.624 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.668 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.585 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.749 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.678 |
MOD_Cter_Amidation | 346 | 349 | PF01082 | 0.703 |
MOD_DYRK1A_RPxSP_1 | 16 | 20 | PF00069 | 0.437 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.743 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.643 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.639 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.817 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.751 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.797 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.612 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.632 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.737 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.699 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.674 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.782 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.822 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.522 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.761 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.761 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.786 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.560 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.668 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.540 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.605 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.678 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.756 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.485 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.585 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.398 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.406 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.769 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.604 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.756 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.544 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.751 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.502 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.739 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.584 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.678 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.448 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.412 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.704 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 71 | 77 | PF00179 | 0.522 |
TRG_DiLeu_BaEn_2 | 229 | 235 | PF01217 | 0.554 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.733 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I155 | Leptomonas seymouri | 47% | 100% |
A0A3Q8I8I3 | Leishmania donovani | 91% | 100% |
A4H774 | Leishmania braziliensis | 71% | 100% |
A4HVL4 | Leishmania infantum | 91% | 100% |
E9APB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |