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: 3 |
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: E9AEY5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.682 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.758 |
CLV_PCSK_PC7_1 | 240 | 246 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.678 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.475 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.610 |
DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 31 | 39 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 312 | 321 | PF00069 | 0.600 |
DOC_MAPK_NFAT4_5 | 111 | 119 | PF00069 | 0.402 |
DOC_MAPK_RevD_3 | 323 | 338 | PF00069 | 0.684 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.620 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.738 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 146 | 154 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 312 | 321 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 341 | 350 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_BIR_III_4 | 392 | 396 | PF00653 | 0.734 |
LIG_BIR_III_4 | 418 | 422 | PF00653 | 0.701 |
LIG_deltaCOP1_diTrp_1 | 159 | 165 | PF00928 | 0.423 |
LIG_eIF4E_1 | 34 | 40 | PF01652 | 0.360 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.725 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.692 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.721 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.553 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.644 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.689 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.756 |
LIG_LIR_Gen_1 | 11 | 21 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 159 | 166 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.734 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.403 |
LIG_PDZ_Class_2 | 453 | 458 | PF00595 | 0.607 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.691 |
LIG_SH2_PTP2 | 34 | 37 | PF00017 | 0.554 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.452 |
LIG_SH3_1 | 247 | 253 | PF00018 | 0.801 |
LIG_SH3_2 | 355 | 360 | PF14604 | 0.555 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.625 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.801 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.581 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.689 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.638 |
LIG_SUMO_SIM_anti_2 | 318 | 323 | PF11976 | 0.570 |
LIG_TRAF2_2 | 225 | 230 | PF00917 | 0.746 |
LIG_UBA3_1 | 440 | 448 | PF00899 | 0.682 |
LIG_WW_3 | 357 | 361 | PF00397 | 0.711 |
MOD_CAAXbox | 455 | 458 | PF01239 | 0.603 |
MOD_CDK_SPK_2 | 351 | 356 | PF00069 | 0.569 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.582 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.556 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.670 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.461 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.595 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.495 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.425 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.686 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.754 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.707 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.712 |
MOD_Cter_Amidation | 261 | 264 | PF01082 | 0.585 |
MOD_GlcNHglycan | 102 | 106 | PF01048 | 0.573 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.426 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.555 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.466 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.785 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.560 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.673 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.677 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.771 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.587 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.458 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.336 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.396 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.560 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.712 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.722 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.601 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.647 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.722 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.735 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.652 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.612 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.732 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.516 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.652 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.749 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.514 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.570 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.557 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.805 |
MOD_PK_1 | 420 | 426 | PF00069 | 0.623 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.462 |
MOD_PKA_1 | 447 | 453 | PF00069 | 0.571 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.485 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.594 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.615 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.582 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.550 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.604 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.462 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.763 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.776 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.646 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.634 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.707 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.601 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.554 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.762 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P595 | Leptomonas seymouri | 39% | 91% |
A0A3S7X927 | Leishmania donovani | 81% | 96% |
A4HMI4 | Leishmania braziliensis | 49% | 100% |
A4IB64 | Leishmania infantum | 81% | 96% |
E9B641 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |