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: A4HUM2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.630 |
CLV_PCSK_PC7_1 | 189 | 195 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.553 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.669 |
DOC_CDC14_PxL_1 | 278 | 286 | PF14671 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 173 | 179 | PF00134 | 0.595 |
DOC_MAPK_DCC_7 | 113 | 121 | PF00069 | 0.677 |
DOC_MAPK_DCC_7 | 62 | 71 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 12 | 20 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 228 | 234 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 59 | 69 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 83 | 93 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 113 | 121 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 14 | 22 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 155 | 162 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 62 | 71 | PF00069 | 0.457 |
DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.791 |
DOC_PP4_FxxP_1 | 419 | 422 | PF00568 | 0.589 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.589 |
DOC_USP7_MATH_2 | 231 | 237 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.786 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_2 | 3 | 9 | PF00533 | 0.524 |
LIG_EH1_1 | 60 | 68 | PF00400 | 0.403 |
LIG_eIF4E_1 | 334 | 340 | PF01652 | 0.672 |
LIG_EVH1_1 | 419 | 423 | PF00568 | 0.587 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.633 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.652 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.749 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.527 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.547 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.569 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.547 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.520 |
LIG_GBD_Chelix_1 | 127 | 135 | PF00786 | 0.459 |
LIG_LIR_Gen_1 | 374 | 384 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.572 |
LIG_LYPXL_yS_3 | 275 | 278 | PF13949 | 0.498 |
LIG_LYPXL_yS_3 | 293 | 296 | PF13949 | 0.515 |
LIG_NRBOX | 262 | 268 | PF00104 | 0.488 |
LIG_Pex14_1 | 226 | 230 | PF04695 | 0.444 |
LIG_PTB_Apo_2 | 55 | 62 | PF02174 | 0.651 |
LIG_Rb_LxCxE_1 | 72 | 92 | PF01857 | 0.538 |
LIG_RPA_C_Fungi | 310 | 322 | PF08784 | 0.703 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.493 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.636 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.505 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.678 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.754 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.675 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.560 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.590 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.482 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.589 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.534 |
LIG_TRAF2_2 | 104 | 109 | PF00917 | 0.571 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.614 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.589 |
LIG_WRC_WIRS_1 | 353 | 358 | PF05994 | 0.643 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.702 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.718 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.590 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.471 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.461 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.529 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.561 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.735 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.591 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.572 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.570 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.608 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.577 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.464 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.642 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.644 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.558 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.628 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.734 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.436 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.634 |
MOD_NEK2_2 | 237 | 242 | PF00069 | 0.586 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.558 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.605 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.470 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.595 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.784 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.484 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.534 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.651 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.502 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.590 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.585 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.700 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.748 |
MOD_SUMO_rev_2 | 150 | 157 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_2 | 2 | 8 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_4 | 268 | 274 | PF01217 | 0.615 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 347 | 352 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 214 | 227 | PF08389 | 0.482 |
TRG_NLS_Bipartite_1 | 83 | 101 | PF00514 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 393 | 398 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA4 | Leptomonas seymouri | 47% | 100% |
A0A3Q8IHA3 | Leishmania donovani | 100% | 100% |
A4H698 | Leishmania braziliensis | 70% | 100% |
E9ANC0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QHA4 | Leishmania major | 90% | 100% |