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: A4HPT5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.492 |
CLV_PCSK_FUR_1 | 3 | 7 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.603 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 209 | 213 | PF12436 | 0.603 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.687 |
DOC_USP7_UBL2_3 | 86 | 90 | PF12436 | 0.608 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.687 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.498 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.590 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.625 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.621 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.616 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.530 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.482 |
LIG_SH2_GRB2like | 72 | 75 | PF00017 | 0.525 |
LIG_SH2_SRC | 240 | 243 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.582 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.562 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.552 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.474 |
MOD_CDK_SPxxK_3 | 202 | 209 | PF00069 | 0.534 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.645 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.580 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.613 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.700 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.542 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.622 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.623 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.444 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.529 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.667 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.551 |
MOD_Cter_Amidation | 183 | 186 | PF01082 | 0.427 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.654 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.524 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.572 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.552 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.636 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.527 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.475 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.705 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.614 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.422 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.675 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.604 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.679 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.658 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.665 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.653 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.522 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.678 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.420 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.497 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.633 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.571 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.649 |
MOD_PKA_1 | 185 | 191 | PF00069 | 0.468 |
MOD_PKA_1 | 310 | 316 | PF00069 | 0.510 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.533 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.426 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.514 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.650 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.518 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.419 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.580 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.613 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.543 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.564 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.529 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 256 | 263 | PF00179 | 0.528 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.528 |
TRG_NLS_Bipartite_1 | 5 | 25 | PF00514 | 0.690 |
TRG_NLS_MonoExtN_4 | 20 | 25 | PF00514 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X1 | Leptomonas seymouri | 38% | 90% |
A0A3Q8IIX5 | Leishmania donovani | 58% | 100% |
A4IE57 | Leishmania infantum | 58% | 100% |
E9ATK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 99% |
Q4Q0Z8 | Leishmania major | 61% | 99% |