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: Q4QAQ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.584 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.569 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.525 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.558 |
DOC_ANK_TNKS_1 | 151 | 158 | PF00023 | 0.686 |
DOC_MAPK_gen_1 | 186 | 196 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.575 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.650 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.662 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.692 |
LIG_ActinCP_TwfCPI_2 | 230 | 239 | PF01115 | 0.619 |
LIG_BIR_III_4 | 245 | 249 | PF00653 | 0.649 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.654 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.611 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.539 |
LIG_Integrin_isoDGR_2 | 4 | 6 | PF01839 | 0.500 |
LIG_Integrin_RGD_1 | 285 | 287 | PF01839 | 0.627 |
LIG_LIR_Apic_2 | 106 | 111 | PF02991 | 0.650 |
LIG_LIR_Apic_2 | 228 | 233 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 7 | 15 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.574 |
LIG_PCNA_yPIPBox_3 | 83 | 91 | PF02747 | 0.485 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.641 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.645 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.581 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.812 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.618 |
LIG_SH3_1 | 299 | 305 | PF00018 | 0.548 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.569 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.563 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.659 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.525 |
LIG_TYR_ITIM | 209 | 214 | PF00017 | 0.561 |
MOD_CDC14_SPxK_1 | 112 | 115 | PF00782 | 0.517 |
MOD_CDK_SPxK_1 | 109 | 115 | PF00069 | 0.511 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.611 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.683 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.658 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.586 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.529 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.545 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.599 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.445 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.626 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.642 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.641 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.631 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.657 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.709 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.532 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.573 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.571 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.646 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.575 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.566 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.586 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.597 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.610 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.568 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.539 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.644 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.513 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.534 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.738 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.679 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.560 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.672 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.581 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.665 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G1 | Leptomonas seymouri | 40% | 100% |
A0A3Q8IBA4 | Leishmania donovani | 85% | 99% |
A4HDD6 | Leishmania braziliensis | 69% | 100% |
A4I0R7 | Leishmania infantum | 85% | 99% |
E9AWR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |