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: A4IE57
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 110 | 114 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.782 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.548 |
DEG_SPOP_SBC_1 | 198 | 202 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.631 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 23 | 28 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.524 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.752 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.515 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.644 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.567 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.559 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.556 |
LIG_SH2_SRC | 283 | 286 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.614 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.559 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.563 |
LIG_WRC_WIRS_1 | 205 | 210 | PF05994 | 0.549 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.588 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.592 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.649 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.627 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.647 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.622 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.586 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.578 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.542 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.641 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.653 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.539 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.476 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.723 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.595 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.559 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.609 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.632 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.521 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.699 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.570 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.566 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.597 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.629 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.604 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.592 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.805 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.573 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.602 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.557 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.584 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.636 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.613 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.628 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.608 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.606 |
MOD_PKB_1 | 252 | 260 | PF00069 | 0.581 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.598 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.491 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.558 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.621 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_4 | 151 | 157 | PF01217 | 0.568 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.519 |
TRG_NLS_Bipartite_1 | 5 | 25 | PF00514 | 0.649 |
TRG_NLS_Bipartite_1 | 91 | 113 | PF00514 | 0.633 |
TRG_NLS_MonoCore_2 | 18 | 23 | PF00514 | 0.574 |
TRG_NLS_MonoExtC_3 | 108 | 113 | PF00514 | 0.591 |
TRG_NLS_MonoExtC_3 | 18 | 23 | PF00514 | 0.561 |
TRG_NLS_MonoExtN_4 | 107 | 113 | PF00514 | 0.590 |
TRG_NLS_MonoExtN_4 | 19 | 25 | PF00514 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X1 | Leptomonas seymouri | 40% | 89% |
A0A3Q8IIX5 | Leishmania donovani | 99% | 100% |
A4HPT5 | Leishmania braziliensis | 58% | 98% |
E9ATK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q0Z8 | Leishmania major | 84% | 100% |