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: A0A3Q8IV47
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.717 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.798 |
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.793 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.601 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.657 |
CLV_PCSK_FUR_1 | 426 | 430 | PF00082 | 0.622 |
CLV_PCSK_FUR_1 | 445 | 449 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 392 | 398 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.773 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.783 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.639 |
DEG_SCF_FBW7_1 | 361 | 367 | PF00400 | 0.733 |
DEG_SCF_FBW7_2 | 84 | 89 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 201 | 205 | PF00917 | 0.742 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.658 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.735 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.797 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.763 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.587 |
DOC_USP7_UBL2_3 | 60 | 64 | PF12436 | 0.695 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.758 |
LIG_BIR_III_2 | 335 | 339 | PF00653 | 0.695 |
LIG_eIF4E_1 | 323 | 329 | PF01652 | 0.640 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.754 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.803 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.674 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.819 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.632 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.766 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.825 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.773 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.591 |
LIG_LIR_Gen_1 | 376 | 386 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.685 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.719 |
LIG_SH2_GRB2like | 323 | 326 | PF00017 | 0.738 |
LIG_SH2_STAT3 | 212 | 215 | PF00017 | 0.775 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.738 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.622 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.690 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.700 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.767 |
LIG_SUMO_SIM_anti_2 | 375 | 384 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 123 | 129 | PF11976 | 0.606 |
MOD_CDK_SPK_2 | 112 | 117 | PF00069 | 0.619 |
MOD_CDK_SPK_2 | 360 | 365 | PF00069 | 0.735 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.729 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.713 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.774 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.589 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.704 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.651 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.662 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.739 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.752 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.755 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.612 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.753 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.599 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.583 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.716 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.788 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.736 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.676 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.748 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.735 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.614 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.796 |
MOD_LATS_1 | 47 | 53 | PF00433 | 0.673 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.559 |
MOD_N-GLC_2 | 393 | 395 | PF02516 | 0.434 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.731 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.766 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.770 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.585 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.789 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.583 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.546 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.717 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.728 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.779 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.637 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.622 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.680 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.473 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.584 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.652 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.538 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.648 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.777 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.656 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.749 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.630 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.703 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.798 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.630 |
MOD_SUMO_rev_2 | 381 | 391 | PF00179 | 0.544 |
TRG_DiLeu_BaEn_3 | 377 | 383 | PF01217 | 0.643 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.691 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.576 |
TRG_NLS_Bipartite_1 | 428 | 448 | PF00514 | 0.571 |
TRG_NLS_MonoCore_2 | 443 | 448 | PF00514 | 0.613 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.713 |
TRG_NLS_MonoExtC_3 | 388 | 394 | PF00514 | 0.544 |
TRG_NLS_MonoExtC_3 | 395 | 400 | PF00514 | 0.472 |
TRG_NLS_MonoExtC_3 | 443 | 448 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 296 | 302 | PF00514 | 0.715 |
TRG_NLS_MonoExtN_4 | 388 | 393 | PF00514 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V5 | Leptomonas seymouri | 36% | 88% |
A4HMF8 | Leishmania braziliensis | 56% | 100% |
A4IB29 | Leishmania infantum | 99% | 100% |
E9AEV9 | Leishmania major | 89% | 100% |
E9B615 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |