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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4IAJ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.805 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.621 |
CLV_Separin_Metazoa | 169 | 173 | PF03568 | 0.659 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.346 |
DEG_SCF_FBW7_1 | 332 | 338 | PF00400 | 0.613 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.681 |
DOC_CYCLIN_RxL_1 | 9 | 19 | PF00134 | 0.417 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 228 | 232 | PF12436 | 0.722 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.772 |
LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 400 | 410 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 437 | 444 | PF00244 | 0.641 |
LIG_BIR_III_2 | 317 | 321 | PF00653 | 0.519 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.658 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.479 |
LIG_EVH1_1 | 329 | 333 | PF00568 | 0.581 |
LIG_EVH1_2 | 319 | 323 | PF00568 | 0.553 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.572 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.490 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.581 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.449 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.804 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.452 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.624 |
LIG_LYPXL_yS_3 | 110 | 113 | PF13949 | 0.621 |
LIG_MLH1_MIPbox_1 | 363 | 367 | PF16413 | 0.479 |
LIG_PCNA_PIPBox_1 | 360 | 369 | PF02747 | 0.511 |
LIG_PCNA_yPIPBox_3 | 2 | 12 | PF02747 | 0.331 |
LIG_PDZ_Class_1 | 483 | 488 | PF00595 | 0.524 |
LIG_PTB_Apo_2 | 387 | 394 | PF02174 | 0.444 |
LIG_REV1ctd_RIR_1 | 480 | 488 | PF16727 | 0.581 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.409 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.437 |
LIG_SH3_2 | 221 | 226 | PF14604 | 0.639 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.578 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.697 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.645 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.655 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.664 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.682 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.742 |
LIG_SH3_4 | 219 | 226 | PF00018 | 0.710 |
LIG_SUMO_SIM_par_1 | 3 | 11 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.578 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.584 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.490 |
LIG_UBA3_1 | 198 | 203 | PF00899 | 0.601 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 479 | 484 | PF05994 | 0.564 |
LIG_WW_3 | 169 | 173 | PF00397 | 0.659 |
LIG_WW_3 | 219 | 223 | PF00397 | 0.583 |
MOD_CDK_SPK_2 | 190 | 195 | PF00069 | 0.635 |
MOD_CDK_SPxK_1 | 333 | 339 | PF00069 | 0.700 |
MOD_CDK_SPxK_1 | 431 | 437 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 471 | 477 | PF00069 | 0.560 |
MOD_CDK_SPxxK_3 | 188 | 195 | PF00069 | 0.575 |
MOD_CDK_SPxxK_3 | 333 | 340 | PF00069 | 0.703 |
MOD_CDK_SPxxK_3 | 431 | 438 | PF00069 | 0.742 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.695 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.575 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.716 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.666 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.794 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.658 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.653 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.600 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.568 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.522 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.804 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.600 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.598 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.600 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.455 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.501 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.640 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.670 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.646 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.391 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.651 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.533 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.602 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.634 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.619 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.559 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.647 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.562 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.610 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.447 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.542 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.774 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.683 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.516 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.570 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.627 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.619 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.621 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.412 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.572 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.615 |
MOD_NEK2_2 | 475 | 480 | PF00069 | 0.558 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.467 |
MOD_PKA_1 | 184 | 190 | PF00069 | 0.570 |
MOD_PKA_1 | 247 | 253 | PF00069 | 0.584 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.643 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.614 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.674 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.613 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.567 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.666 |
MOD_Plk_2-3 | 408 | 414 | PF00069 | 0.398 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.475 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.398 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.516 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.681 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.835 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.681 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.600 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.668 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.620 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.578 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.766 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.741 |
MOD_SUMO_for_1 | 231 | 234 | PF00179 | 0.600 |
MOD_SUMO_for_1 | 386 | 389 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 138 | 148 | PF00179 | 0.627 |
MOD_SUMO_rev_2 | 381 | 388 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_2 | 388 | 394 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.620 |
TRG_NLS_MonoCore_2 | 208 | 213 | PF00514 | 0.634 |
TRG_NLS_MonoExtC_3 | 208 | 214 | PF00514 | 0.635 |
TRG_NLS_MonoExtN_4 | 244 | 251 | PF00514 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYZ0 | Leptomonas seymouri | 46% | 95% |
A0A1X0PAH9 | Trypanosomatidae | 28% | 93% |
A0A3S7X8I7 | Leishmania donovani | 100% | 100% |
A4HBE4 | Leishmania braziliensis | 64% | 99% |
E9B5L6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q2C0 | Leishmania major | 86% | 100% |