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: A4I0Q9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.778 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.629 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.621 |
DEG_SCF_FBW7_1 | 93 | 98 | PF00400 | 0.591 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.597 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 123 | PF00134 | 0.465 |
DOC_MAPK_DCC_7 | 103 | 112 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 31 | 40 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 103 | 112 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.475 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.540 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.752 |
LIG_14-3-3_CanoR_1 | 124 | 134 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.673 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.674 |
LIG_CaM_NSCaTE_8 | 82 | 89 | PF13499 | 0.593 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.492 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.434 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.563 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.690 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.543 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.719 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.700 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.613 |
LIG_PDZ_Class_3 | 433 | 438 | PF00595 | 0.412 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.496 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.617 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.574 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.658 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.591 |
LIG_SH3_2 | 170 | 175 | PF14604 | 0.501 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.687 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.448 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.505 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.573 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.714 |
LIG_SUMO_SIM_anti_2 | 6 | 11 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 106 | 113 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.619 |
LIG_UBA3_1 | 262 | 267 | PF00899 | 0.520 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.604 |
MOD_CDK_SPxK_1 | 25 | 31 | PF00069 | 0.649 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.664 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.702 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.532 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.597 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.608 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.659 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.583 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.638 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.559 |
MOD_Cter_Amidation | 321 | 324 | PF01082 | 0.787 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.647 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.550 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.728 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.598 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.592 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.596 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.601 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.661 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.534 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.520 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.731 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.619 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.482 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.466 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.471 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.655 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.654 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.701 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.557 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.749 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.704 |
MOD_N-GLC_2 | 307 | 309 | PF02516 | 0.741 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.727 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.594 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.557 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.519 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.440 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.557 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.559 |
MOD_PK_1 | 314 | 320 | PF00069 | 0.633 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.563 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.647 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.587 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.647 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.691 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.636 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.559 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.677 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.619 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.728 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.459 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.464 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.681 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.469 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.650 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.674 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.756 |
TRG_DiLeu_BaEn_1 | 221 | 226 | PF01217 | 0.627 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.606 |
TRG_NES_CRM1_1 | 149 | 161 | PF08389 | 0.463 |
TRG_NLS_MonoCore_2 | 399 | 404 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 398 | 405 | PF00514 | 0.757 |
TRG_Pf-PMV_PEXEL_1 | 223 | 227 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3F4 | Leptomonas seymouri | 43% | 100% |
A0A3S7WY61 | Leishmania donovani | 98% | 100% |
A4HDC8 | Leishmania braziliensis | 72% | 100% |
E9AWR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QAR2 | Leishmania major | 90% | 100% |