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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QIE8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 173 | 177 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 322 | 326 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.823 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.645 |
CLV_PCSK_FUR_1 | 413 | 417 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.823 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.712 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.690 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.577 |
DOC_ANK_TNKS_1 | 104 | 111 | PF00023 | 0.656 |
DOC_MAPK_gen_1 | 413 | 423 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 244 | 251 | PF00069 | 0.686 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.724 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.629 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.586 |
LIG_ActinCP_TwfCPI_2 | 252 | 259 | PF01115 | 0.636 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.723 |
LIG_BIR_III_2 | 218 | 222 | PF00653 | 0.620 |
LIG_BIR_III_2 | 263 | 267 | PF00653 | 0.660 |
LIG_BRCT_BRCA1_1 | 441 | 445 | PF00533 | 0.676 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.740 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.712 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.660 |
LIG_Integrin_RGD_1 | 107 | 109 | PF01839 | 0.679 |
LIG_Integrin_RGD_1 | 192 | 194 | PF01839 | 0.642 |
LIG_LIR_Apic_2 | 31 | 36 | PF02991 | 0.664 |
LIG_LIR_Apic_2 | 406 | 412 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 479 | 490 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.625 |
LIG_MYND_1 | 269 | 273 | PF01753 | 0.673 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.671 |
LIG_PTAP_UEV_1 | 93 | 98 | PF05743 | 0.688 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.620 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.665 |
LIG_SH3_1 | 33 | 39 | PF00018 | 0.618 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.672 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.628 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.618 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.644 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.712 |
LIG_SUMO_SIM_par_1 | 267 | 275 | PF11976 | 0.721 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.721 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.714 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.677 |
LIG_TRFH_1 | 408 | 412 | PF08558 | 0.665 |
LIG_WW_3 | 1 | 5 | PF00397 | 0.643 |
LIG_WW_3 | 143 | 147 | PF00397 | 0.670 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.677 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.785 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.594 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.609 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.654 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.686 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.499 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.689 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.777 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.600 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.694 |
MOD_Cter_Amidation | 176 | 179 | PF01082 | 0.672 |
MOD_DYRK1A_RPxSP_1 | 265 | 269 | PF00069 | 0.652 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.734 |
MOD_GlcNHglycan | 124 | 130 | PF01048 | 0.657 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.685 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.546 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.677 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.725 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.632 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.759 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.754 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.718 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.552 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.630 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.660 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.748 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.757 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.747 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.778 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.729 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.722 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.608 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.676 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.631 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.582 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.680 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.574 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.718 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.654 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.681 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.695 |
MOD_PKA_1 | 299 | 305 | PF00069 | 0.639 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.627 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.653 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.633 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.707 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.604 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.559 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.636 |
MOD_PKB_1 | 182 | 190 | PF00069 | 0.582 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.664 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.661 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.726 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.649 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.617 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.586 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.676 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.661 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.628 |
TRG_NLS_MonoExtC_3 | 212 | 218 | PF00514 | 0.700 |
TRG_NLS_MonoExtN_4 | 210 | 217 | PF00514 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 362 | 367 | PF00026 | 0.669 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H635 | Leishmania donovani | 87% | 100% |
A4H588 | Leishmania braziliensis | 50% | 95% |
A4HTH2 | Leishmania infantum | 87% | 100% |
E9AMA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 97% |