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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B4G4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.536 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.487 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.474 |
DEG_SPOP_SBC_1 | 215 | 219 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.415 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.692 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.536 |
DOC_USP7_UBL2_3 | 108 | 112 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 60 | 64 | PF12436 | 0.577 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.562 |
LIG_eIF4E_1 | 308 | 314 | PF01652 | 0.530 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.487 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.570 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.579 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.574 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.565 |
LIG_PDZ_Class_2 | 381 | 386 | PF00595 | 0.649 |
LIG_SH3_1 | 271 | 277 | PF00018 | 0.547 |
LIG_SH3_2 | 265 | 270 | PF14604 | 0.692 |
LIG_SH3_2 | 317 | 322 | PF14604 | 0.592 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.666 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.651 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.555 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.623 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.684 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.558 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.525 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.702 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.636 |
MOD_CDK_SPK_2 | 264 | 269 | PF00069 | 0.693 |
MOD_CDK_SPxK_1 | 264 | 270 | PF00069 | 0.694 |
MOD_CDK_SPxxK_3 | 264 | 271 | PF00069 | 0.694 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.710 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.375 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.645 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.565 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.608 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.419 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.408 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.626 |
MOD_GlcNHglycan | 238 | 243 | PF01048 | 0.576 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.664 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.578 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.635 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.459 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.707 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.520 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.663 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.609 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.667 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.462 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.559 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.467 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.670 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.658 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.710 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.499 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.524 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.677 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.694 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.698 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.633 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.590 |
MOD_SUMO_for_1 | 14 | 17 | PF00179 | 0.379 |
MOD_SUMO_for_1 | 96 | 99 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 249 | 258 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 99 | 103 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.536 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.401 |
TRG_NLS_Bipartite_1 | 71 | 88 | PF00514 | 0.513 |
TRG_NLS_MonoExtN_4 | 83 | 88 | PF00514 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IUB2 | Leishmania donovani | 78% | 84% |
A4HM33 | Leishmania braziliensis | 53% | 98% |
A4I9G6 | Leishmania infantum | 77% | 84% |
Q4Q3L1 | Leishmania major | 77% | 98% |