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: E9AHP4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.718 |
CLV_C14_Caspase3-7 | 428 | 432 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.709 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 319 | 325 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.593 |
DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.438 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.545 |
DEG_SPOP_SBC_1 | 371 | 375 | PF00917 | 0.620 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.670 |
DOC_SPAK_OSR1_1 | 250 | 254 | PF12202 | 0.499 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.803 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 176 | 186 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 237 | 245 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 335 | 340 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.539 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.683 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.514 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.797 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.500 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.599 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.704 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.545 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.724 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.492 |
LIG_MYND_1 | 70 | 74 | PF01753 | 0.704 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.470 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 258 | 262 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.507 |
LIG_SH3_2 | 171 | 176 | PF14604 | 0.671 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.721 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.641 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.623 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.690 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.713 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.508 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.532 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.445 |
LIG_UBA3_1 | 210 | 215 | PF00899 | 0.720 |
LIG_WW_3 | 170 | 174 | PF00397 | 0.668 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.708 |
MOD_CDK_SPxxK_3 | 403 | 410 | PF00069 | 0.669 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.715 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.735 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.629 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.621 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.768 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.739 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.563 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.504 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.528 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.693 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.457 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.660 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.713 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.432 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.525 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.652 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.794 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.740 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.774 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.608 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.641 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.674 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.756 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.596 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.472 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.439 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.644 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.685 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.735 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.788 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.478 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.463 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.627 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.606 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.402 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.637 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.774 |
MOD_OFUCOSY | 252 | 257 | PF10250 | 0.469 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.591 |
MOD_PK_1 | 335 | 341 | PF00069 | 0.695 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.507 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.781 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.511 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.696 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.637 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.408 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.738 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.536 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.616 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.698 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.440 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.754 |
MOD_SUMO_for_1 | 314 | 317 | PF00179 | 0.746 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.565 |
TRG_NES_CRM1_1 | 417 | 431 | PF08389 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILE8 | Leptomonas seymouri | 48% | 100% |
A0A3Q8IH00 | Leishmania donovani | 99% | 100% |
A4HLT8 | Leishmania braziliensis | 73% | 98% |
D0A688 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B464 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
Q4Q3W2 | Leishmania major | 92% | 99% |