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. | yes | yes: 10 |
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 | yes | yes: 5, no: 1 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QFC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.707 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.715 |
DEG_Kelch_Keap1_1 | 151 | 156 | PF01344 | 0.491 |
DEG_ODPH_VHL_1 | 15 | 26 | PF01847 | 0.564 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.543 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.454 |
DOC_CDC14_PxL_1 | 13 | 21 | PF14671 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 9 | 15 | PF00134 | 0.609 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.454 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.613 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.507 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.574 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.548 |
LIG_CSL_BTD_1 | 119 | 122 | PF09270 | 0.539 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.579 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.648 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.500 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.491 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.472 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.579 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.488 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.510 |
LIG_Integrin_isoDGR_2 | 264 | 266 | PF01839 | 0.720 |
LIG_MYND_1 | 181 | 185 | PF01753 | 0.537 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.562 |
LIG_PCNA_yPIPBox_3 | 188 | 199 | PF02747 | 0.517 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.515 |
LIG_SH2_GRB2like | 205 | 208 | PF00017 | 0.492 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.500 |
LIG_SH2_SRC | 205 | 208 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.489 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.544 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.533 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.587 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.435 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.462 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.543 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.522 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.547 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.533 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.571 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.781 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.804 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.843 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.715 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.681 |
MOD_GlcNHglycan | 48 | 52 | PF01048 | 0.728 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.716 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.615 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.591 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.504 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.542 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.532 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.527 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.454 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.437 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.707 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.784 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.735 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.494 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.551 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.465 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.539 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.703 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.432 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.550 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.582 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.479 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.456 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.524 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.456 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.459 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.571 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.368 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.466 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.552 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.463 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.657 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P748 | Leptomonas seymouri | 40% | 100% |
A0A3S7WTK4 | Leishmania donovani | 89% | 100% |
A4H829 | Leishmania braziliensis | 62% | 100% |
A4HWF5 | Leishmania infantum | 89% | 100% |
E9AQ54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |