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: A0A3Q8ITN7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.804 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.542 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.510 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.615 |
DEG_SPOP_SBC_1 | 339 | 343 | PF00917 | 0.581 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.658 |
DOC_MAPK_gen_1 | 497 | 504 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.632 |
DOC_MAPK_NFAT4_5 | 281 | 289 | PF00069 | 0.554 |
DOC_PP1_RVXF_1 | 305 | 311 | PF00149 | 0.647 |
DOC_PP1_RVXF_1 | 49 | 56 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.534 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.637 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 155 | 164 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 307 | 311 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.481 |
LIG_BIR_III_4 | 391 | 395 | PF00653 | 0.652 |
LIG_EVH1_1 | 502 | 506 | PF00568 | 0.536 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.657 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.415 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.624 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.483 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.630 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.662 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.642 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.567 |
LIG_Integrin_RGD_1 | 57 | 59 | PF01839 | 0.439 |
LIG_LIR_Apic_2 | 198 | 203 | PF02991 | 0.585 |
LIG_LIR_Apic_2 | 227 | 232 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.635 |
LIG_LIR_LC3C_4 | 285 | 288 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.538 |
LIG_PTAP_UEV_1 | 176 | 181 | PF05743 | 0.555 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.454 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.630 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 411 | 415 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.401 |
LIG_SH3_1 | 517 | 523 | PF00018 | 0.592 |
LIG_SH3_2 | 276 | 281 | PF14604 | 0.601 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.631 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.683 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.803 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.619 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.602 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.593 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.760 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.507 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 282 | 289 | PF11976 | 0.633 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.666 |
MOD_CDK_SPK_2 | 215 | 220 | PF00069 | 0.577 |
MOD_CDK_SPK_2 | 296 | 301 | PF00069 | 0.596 |
MOD_CDK_SPK_2 | 509 | 514 | PF00069 | 0.674 |
MOD_CDK_SPK_2 | 66 | 71 | PF00069 | 0.494 |
MOD_CDK_SPxK_1 | 509 | 515 | PF00069 | 0.622 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.614 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.574 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.829 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.730 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.633 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.570 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.601 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.473 |
MOD_Cter_Amidation | 471 | 474 | PF01082 | 0.325 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.626 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.695 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.598 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.501 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.718 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.592 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.740 |
MOD_GlcNHglycan | 391 | 395 | PF01048 | 0.510 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.665 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.698 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.677 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.709 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.555 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.685 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.679 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.650 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.687 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.462 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.679 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.674 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.542 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.479 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.621 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.758 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.640 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.577 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.520 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.606 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.636 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.510 |
MOD_PKB_1 | 193 | 201 | PF00069 | 0.538 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.443 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.575 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.583 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.543 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.729 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.325 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.724 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.548 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.600 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.619 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.689 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.638 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.676 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.586 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.474 |
MOD_SUMO_rev_2 | 391 | 401 | PF00179 | 0.684 |
MOD_SUMO_rev_2 | 544 | 550 | PF00179 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 513 | 515 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 282 | 294 | PF08389 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJN9 | Leptomonas seymouri | 41% | 82% |
A4HKY8 | Leishmania braziliensis | 61% | 100% |
A4I8G9 | Leishmania infantum | 99% | 100% |
E9B3C9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q4S7 | Leishmania major | 89% | 100% |