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: A0A3S7X722
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.759 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.603 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.622 |
DEG_SCF_FBW7_1 | 310 | 315 | PF00400 | 0.697 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.634 |
DOC_ANK_TNKS_1 | 469 | 476 | PF00023 | 0.548 |
DOC_CKS1_1 | 442 | 447 | PF01111 | 0.431 |
DOC_CYCLIN_RxL_1 | 190 | 197 | PF00134 | 0.651 |
DOC_CYCLIN_RxL_1 | 392 | 401 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 519 | 525 | PF00134 | 0.607 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 325 | 332 | PF00244 | 0.831 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.793 |
LIG_AP2alpha_2 | 83 | 85 | PF02296 | 0.678 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.711 |
LIG_BRCT_BRCA1_2 | 69 | 75 | PF00533 | 0.714 |
LIG_deltaCOP1_diTrp_1 | 127 | 131 | PF00928 | 0.617 |
LIG_deltaCOP1_diTrp_1 | 411 | 418 | PF00928 | 0.651 |
LIG_EVH1_2 | 288 | 292 | PF00568 | 0.711 |
LIG_EVH1_2 | 445 | 449 | PF00568 | 0.480 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.520 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.613 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.728 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.392 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.555 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.457 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.480 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.726 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.839 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.511 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.602 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.714 |
LIG_Integrin_RGD_1 | 234 | 236 | PF01839 | 0.740 |
LIG_LIR_Apic_2 | 89 | 94 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.671 |
LIG_LIR_Gen_1 | 38 | 44 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 415 | 425 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.700 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.616 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.511 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.715 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.795 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.506 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.679 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.614 |
LIG_WW_3 | 444 | 448 | PF00397 | 0.500 |
MOD_CDK_SPxK_1 | 441 | 447 | PF00069 | 0.436 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.683 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.660 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.798 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.702 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.606 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.793 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.661 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.637 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.624 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.690 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.660 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.741 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.755 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.626 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.501 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.723 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.663 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.825 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.696 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.719 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.718 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.825 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.634 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.677 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.683 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.689 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.776 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.838 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.780 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.611 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.739 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.627 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.439 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.566 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.688 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.714 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.687 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.793 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.507 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.803 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.608 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.759 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.614 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.599 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.725 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.661 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.629 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.681 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.721 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.692 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.491 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.694 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.529 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.674 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.405 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.699 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.501 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.494 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.474 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.632 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.752 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.759 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.502 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.436 |
MOD_SUMO_rev_2 | 144 | 148 | PF00179 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 191 | 196 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.701 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 510 | 515 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 77 | 82 | PF00026 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF55 | Leptomonas seymouri | 53% | 98% |
A4HLU4 | Leishmania braziliensis | 70% | 100% |
E9AHP9 | Leishmania infantum | 99% | 100% |
E9B470 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q3V6 | Leishmania major | 88% | 100% |