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: Q4QEQ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 154 | 160 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.629 |
CLV_Separin_Metazoa | 21 | 25 | PF03568 | 0.540 |
DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.550 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.416 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.592 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.475 |
DOC_CKS1_1 | 203 | 208 | PF01111 | 0.676 |
DOC_CKS1_1 | 212 | 217 | PF01111 | 0.488 |
DOC_CKS1_1 | 303 | 308 | PF01111 | 0.577 |
DOC_CYCLIN_RxL_1 | 232 | 242 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 212 | 218 | PF00134 | 0.512 |
DOC_CYCLIN_yCln2_LP_2 | 7 | 13 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 396 | 403 | PF00069 | 0.530 |
DOC_MAPK_NFAT4_5 | 396 | 404 | PF00069 | 0.532 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.606 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.498 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.590 |
DOC_PP4_FxxP_1 | 95 | 98 | PF00568 | 0.608 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.514 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 170 | 180 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 331 | 338 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 78 | 86 | PF00244 | 0.538 |
LIG_APCC_ABBA_1 | 23 | 28 | PF00400 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.607 |
LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.447 |
LIG_EVH1_2 | 180 | 184 | PF00568 | 0.641 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.565 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.620 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.628 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.583 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.528 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 92 | 98 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 339 | 350 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.493 |
LIG_MYND_1 | 5 | 9 | PF01753 | 0.496 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.452 |
LIG_PCNA_yPIPBox_3 | 19 | 27 | PF02747 | 0.547 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.563 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.606 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.607 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.586 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.584 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.682 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.590 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.572 |
LIG_UBA3_1 | 249 | 258 | PF00899 | 0.521 |
LIG_WW_2 | 5 | 8 | PF00397 | 0.499 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.570 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.487 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.583 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.617 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.557 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.608 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.494 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.588 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.656 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.389 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.429 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.658 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.563 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.591 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.522 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.411 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.489 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.624 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.659 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.617 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.518 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.598 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.547 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.494 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.622 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.592 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.524 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.697 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.689 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.625 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.520 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.632 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.602 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.555 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.424 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.659 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.591 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.623 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.548 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.504 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.712 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.699 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.623 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.590 |
MOD_PKB_1 | 436 | 444 | PF00069 | 0.614 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.536 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.468 |
MOD_Plk_2-3 | 136 | 142 | PF00069 | 0.651 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.677 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.404 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.557 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.522 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.559 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.607 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.689 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.481 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.600 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.545 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.655 |
TRG_DiLeu_BaEn_1 | 38 | 43 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.613 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.585 |
TRG_DiLeu_LyEn_5 | 38 | 43 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.611 |
TRG_NLS_MonoCore_2 | 319 | 324 | PF00514 | 0.596 |
TRG_NLS_MonoCore_2 | 434 | 439 | PF00514 | 0.646 |
TRG_NLS_MonoExtC_3 | 319 | 324 | PF00514 | 0.616 |
TRG_NLS_MonoExtC_3 | 434 | 440 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 432 | 439 | PF00514 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q0 | Leptomonas seymouri | 30% | 100% |
A0A3Q8IAM2 | Leishmania donovani | 90% | 100% |
A4H8P3 | Leishmania braziliensis | 73% | 100% |
A4HX13 | Leishmania infantum | 90% | 100% |
E9AQS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |