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: A0A3S7WY61
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.797 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.624 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.400 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.458 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.518 |
DEG_SCF_FBW7_1 | 93 | 98 | PF00400 | 0.595 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.667 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 123 | PF00134 | 0.362 |
DOC_MAPK_DCC_7 | 103 | 112 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 103 | 112 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.403 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.586 |
DOC_PP2B_PxIxI_1 | 107 | 113 | PF00149 | 0.264 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 124 | 134 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.692 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.565 |
LIG_CaM_NSCaTE_8 | 82 | 89 | PF13499 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 430 | 433 | PF00928 | 0.319 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.421 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.376 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.394 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.569 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.444 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.605 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.613 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.430 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.457 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.493 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.496 |
LIG_SH3_2 | 170 | 175 | PF14604 | 0.399 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.695 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.337 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.399 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.518 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 6 | 11 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 106 | 113 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.510 |
LIG_UBA3_1 | 262 | 267 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.451 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.566 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.540 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.486 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.555 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.451 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.643 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.528 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.479 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.416 |
MOD_Cter_Amidation | 321 | 324 | PF01082 | 0.793 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.550 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.328 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.709 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.556 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.478 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.406 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.598 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.564 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.462 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.467 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.592 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.571 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.622 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.323 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.543 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.559 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.481 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.501 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.651 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.500 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.598 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.591 |
MOD_N-GLC_2 | 307 | 309 | PF02516 | 0.589 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.572 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.541 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.443 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.485 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.496 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.378 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.388 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.452 |
MOD_PK_1 | 314 | 320 | PF00069 | 0.543 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.523 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.493 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.542 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.586 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.545 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.609 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.503 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.563 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.566 |
MOD_Plk_2-3 | 383 | 389 | PF00069 | 0.483 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.512 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.474 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.438 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.564 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.356 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.562 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.570 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.664 |
TRG_DiLeu_BaEn_1 | 221 | 226 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 149 | 161 | PF08389 | 0.359 |
TRG_NLS_MonoCore_2 | 399 | 404 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 398 | 405 | PF00514 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3F4 | Leptomonas seymouri | 43% | 100% |
A4HDC8 | Leishmania braziliensis | 72% | 100% |
A4I0Q9 | Leishmania infantum | 98% | 100% |
E9AWR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QAR2 | Leishmania major | 90% | 100% |