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: E9ALL6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.492 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.464 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.501 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.552 |
DOC_MAPK_DCC_7 | 37 | 46 | PF00069 | 0.752 |
DOC_MAPK_gen_1 | 245 | 255 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 406 | 414 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 192 | 201 | PF00069 | 0.728 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.752 |
DOC_MAPK_NFAT4_5 | 250 | 258 | PF00069 | 0.583 |
DOC_PP4_FxxP_1 | 440 | 443 | PF00568 | 0.652 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.775 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 235 | 244 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 356 | 365 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 98 | 102 | PF00244 | 0.718 |
LIG_Actin_WH2_2 | 358 | 373 | PF00022 | 0.516 |
LIG_FAT_LD_1 | 130 | 138 | PF03623 | 0.552 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.714 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.753 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.734 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.565 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.592 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.745 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.706 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.741 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.530 |
LIG_GBD_Chelix_1 | 129 | 137 | PF00786 | 0.382 |
LIG_LIR_Apic_2 | 437 | 443 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 212 | 218 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.611 |
LIG_MAD2 | 16 | 24 | PF02301 | 0.657 |
LIG_NRBOX | 92 | 98 | PF00104 | 0.646 |
LIG_PTB_Apo_2 | 256 | 263 | PF02174 | 0.521 |
LIG_PTB_Phospho_1 | 256 | 262 | PF10480 | 0.437 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.474 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.620 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.650 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.625 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.675 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.775 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.654 |
LIG_SUMO_SIM_anti_2 | 315 | 324 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 200 | 207 | PF11976 | 0.672 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.745 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.504 |
MOD_CDK_SPK_2 | 380 | 385 | PF00069 | 0.598 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.674 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.690 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.712 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.763 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.725 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.767 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.734 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.735 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.667 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.738 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.537 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.765 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.787 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.529 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.559 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.743 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.711 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.645 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.697 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.733 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.787 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.479 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.682 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.598 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.635 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.707 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.623 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.479 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.655 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.687 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.601 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.493 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.465 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.631 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.775 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.649 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.597 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.837 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.625 |
MOD_PK_1 | 56 | 62 | PF00069 | 0.493 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.584 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.811 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.764 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.538 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.755 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.826 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.707 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.716 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.762 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.674 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.601 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.459 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.727 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.507 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.672 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.487 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.739 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.633 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.586 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.671 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.741 |
TRG_ER_diArg_1 | 221 | 224 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.764 |
TRG_NLS_MonoCore_2 | 283 | 288 | PF00514 | 0.622 |
TRG_NLS_MonoExtC_3 | 283 | 288 | PF00514 | 0.719 |
TRG_NLS_MonoExtN_4 | 284 | 290 | PF00514 | 0.718 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW7 | Leptomonas seymouri | 30% | 100% |
A0A3Q8IRH8 | Leishmania donovani | 79% | 100% |
A4HHK6 | Leishmania braziliensis | 53% | 94% |
A4I4R7 | Leishmania infantum | 79% | 100% |
E9AE69 | Leishmania major | 76% | 99% |