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: Q4Q787
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 123 | 127 | PF00082 | 0.690 |
CLV_PCSK_FUR_1 | 152 | 156 | PF00082 | 0.588 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.599 |
CLV_PCSK_PC7_1 | 133 | 139 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.613 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.619 |
DEG_SCF_FBW7_1 | 111 | 116 | PF00400 | 0.704 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.510 |
DOC_CKS1_1 | 127 | 132 | PF01111 | 0.632 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.756 |
DOC_MAPK_DCC_7 | 196 | 204 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.629 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.541 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.582 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.571 |
LIG_deltaCOP1_diTrp_1 | 243 | 248 | PF00928 | 0.606 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.606 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.654 |
LIG_LIR_Gen_1 | 18 | 24 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 302 | 311 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.461 |
LIG_PCNA_yPIPBox_3 | 173 | 187 | PF02747 | 0.598 |
LIG_SH2_PTP2 | 127 | 130 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.656 |
LIG_SH3_1 | 278 | 284 | PF00018 | 0.563 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.691 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.666 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.540 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.496 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.682 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.690 |
LIG_SH3_4 | 192 | 199 | PF00018 | 0.643 |
LIG_SH3_4 | 205 | 212 | PF00018 | 0.661 |
LIG_SUMO_SIM_par_1 | 273 | 279 | PF11976 | 0.586 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.663 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.541 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.703 |
MOD_CDK_SPxxK_3 | 126 | 133 | PF00069 | 0.635 |
MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.564 |
MOD_CDK_SPxxK_3 | 294 | 301 | PF00069 | 0.505 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.657 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.587 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.716 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.663 |
MOD_Cter_Amidation | 290 | 293 | PF01082 | 0.609 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.585 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.646 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.562 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.392 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.581 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.613 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.512 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.542 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.616 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.486 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.594 |
MOD_PK_1 | 162 | 168 | PF00069 | 0.710 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.517 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.596 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.388 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.614 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.527 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.546 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.740 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.785 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.578 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.508 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.468 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.661 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.640 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.654 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.472 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.620 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.696 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.587 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.643 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.628 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 35 | 40 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 6 | 10 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P913 | Leptomonas seymouri | 61% | 100% |
A0A1X0P1U3 | Trypanosomatidae | 30% | 100% |
A0A3Q8IFW1 | Leishmania donovani | 93% | 100% |
A0A422P3E4 | Trypanosoma rangeli | 33% | 100% |
A4HID8 | Leishmania braziliensis | 76% | 99% |
A4I5N5 | Leishmania infantum | 93% | 100% |
C9ZR04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B0X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BYT6 | Trypanosoma cruzi | 33% | 99% |