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: Q4Q0Z8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.683 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.776 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.598 |
DEG_SPOP_SBC_1 | 197 | 201 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.577 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.607 |
DOC_USP7_UBL2_3 | 214 | 218 | PF12436 | 0.635 |
DOC_USP7_UBL2_3 | 87 | 91 | PF12436 | 0.604 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.562 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.774 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.469 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.634 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.704 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.646 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.601 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.448 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.507 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.636 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.578 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.547 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.523 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.560 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.571 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.591 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.588 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.657 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.714 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.599 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.634 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.569 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.568 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.399 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.636 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.653 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.561 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.515 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.621 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.585 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.559 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.576 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.578 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.634 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.588 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.587 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.672 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.580 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.624 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.653 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.739 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.640 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.578 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.582 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.629 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.546 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.529 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.625 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.612 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.655 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.605 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.647 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.609 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.585 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.608 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.622 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.554 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.590 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.436 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.399 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.593 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.608 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.547 |
TRG_DiLeu_BaEn_4 | 150 | 156 | PF01217 | 0.534 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.624 |
TRG_NLS_Bipartite_1 | 5 | 25 | PF00514 | 0.672 |
TRG_NLS_Bipartite_1 | 91 | 113 | PF00514 | 0.644 |
TRG_NLS_MonoCore_2 | 19 | 24 | PF00514 | 0.576 |
TRG_NLS_MonoCore_2 | 4 | 9 | PF00514 | 0.561 |
TRG_NLS_MonoExtN_4 | 20 | 25 | PF00514 | 0.618 |
TRG_NLS_MonoExtN_4 | 3 | 9 | PF00514 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.688 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X1 | Leptomonas seymouri | 41% | 89% |
A0A3Q8IIX5 | Leishmania donovani | 85% | 100% |
A4HPT5 | Leishmania braziliensis | 61% | 100% |
A4IE57 | Leishmania infantum | 84% | 100% |
E9ATK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |