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: A4HJJ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.820 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.618 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.586 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.541 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.693 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 273 | 278 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.792 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.567 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.505 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.529 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.569 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.796 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.689 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.609 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.566 |
LIG_LIR_Apic_2 | 218 | 224 | PF02991 | 0.779 |
LIG_LIR_Apic_2 | 329 | 333 | PF02991 | 0.570 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.558 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.725 |
LIG_LIR_Gen_1 | 155 | 161 | PF02991 | 0.528 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.752 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.555 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.755 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.722 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.543 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.737 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.766 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.603 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.577 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.571 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.564 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.619 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.626 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.749 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.576 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.552 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.593 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.769 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.572 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.567 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.631 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.580 |
MOD_Cter_Amidation | 385 | 388 | PF01082 | 0.784 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.586 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.634 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.622 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.725 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.727 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.728 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.627 |
MOD_GlcNHglycan | 337 | 341 | PF01048 | 0.790 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.544 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.601 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.689 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.682 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.597 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.657 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.763 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.658 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.754 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.633 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.716 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.712 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.670 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.626 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.712 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.629 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.759 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.638 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.712 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.661 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.746 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.538 |
MOD_PK_1 | 273 | 279 | PF00069 | 0.566 |
MOD_PKA_1 | 273 | 279 | PF00069 | 0.649 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.630 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.794 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.653 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.625 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.565 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.765 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.767 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.553 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.568 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.518 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.631 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.620 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.651 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.683 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.625 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.719 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.766 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.607 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.766 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.718 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.763 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.655 |
MOD_SUMO_for_1 | 313 | 316 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 276 | 285 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_4 | 32 | 38 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.534 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILC0 | Leptomonas seymouri | 35% | 94% |
A0A3S5H7Q3 | Leishmania donovani | 57% | 100% |
A4I6Z0 | Leishmania infantum | 54% | 100% |
E9AEF6 | Leishmania major | 58% | 97% |
E9B211 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |