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: Q4Q385
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.518 |
DEG_SCF_FBW7_1 | 139 | 145 | PF00400 | 0.656 |
DEG_SCF_FBW7_1 | 230 | 237 | PF00400 | 0.534 |
DEG_SCF_FBW7_2 | 378 | 385 | PF00400 | 0.501 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.658 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.533 |
DOC_CKS1_1 | 345 | 350 | PF01111 | 0.695 |
DOC_CKS1_1 | 379 | 384 | PF01111 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.615 |
DOC_MAPK_gen_1 | 207 | 217 | PF00069 | 0.571 |
DOC_MAPK_HePTP_8 | 154 | 166 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 157 | 166 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 210 | 217 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 452 | 460 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.572 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 191 | 195 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 553 | 557 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.611 |
LIG_BIR_III_2 | 341 | 345 | PF00653 | 0.636 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.533 |
LIG_CaM_IQ_9 | 53 | 68 | PF13499 | 0.585 |
LIG_deltaCOP1_diTrp_1 | 361 | 372 | PF00928 | 0.600 |
LIG_eIF4E_1 | 182 | 188 | PF01652 | 0.641 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.580 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.593 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.553 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.412 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.656 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.490 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.481 |
LIG_GSK3_LRP6_1 | 142 | 147 | PF00069 | 0.626 |
LIG_LIR_Apic_2 | 331 | 336 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 414 | 424 | PF02991 | 0.457 |
LIG_LIR_LC3C_4 | 537 | 541 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.491 |
LIG_NRBOX | 583 | 589 | PF00104 | 0.526 |
LIG_Pex14_2 | 372 | 376 | PF04695 | 0.593 |
LIG_PTAP_UEV_1 | 202 | 207 | PF05743 | 0.536 |
LIG_Rb_LxCxE_1 | 43 | 59 | PF01857 | 0.499 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 322 | 326 | PF00017 | 0.546 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.376 |
LIG_SH3_1 | 136 | 142 | PF00018 | 0.667 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.631 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.586 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.625 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.555 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.530 |
LIG_SUMO_SIM_anti_2 | 537 | 542 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 152 | 158 | PF11976 | 0.461 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.668 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.525 |
LIG_TRFH_1 | 254 | 258 | PF08558 | 0.654 |
LIG_TYR_ITIM | 180 | 185 | PF00017 | 0.482 |
LIG_TYR_ITIM | 320 | 325 | PF00017 | 0.547 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.427 |
MOD_CDK_SPK_2 | 135 | 140 | PF00069 | 0.648 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.626 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.668 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.538 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.634 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.584 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.707 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.473 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.657 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.609 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.542 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.571 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.659 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.619 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.647 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.566 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.485 |
MOD_Cter_Amidation | 337 | 340 | PF01082 | 0.601 |
MOD_DYRK1A_RPxSP_1 | 452 | 456 | PF00069 | 0.548 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.564 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.519 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.606 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.686 |
MOD_GlcNHglycan | 246 | 252 | PF01048 | 0.594 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.493 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.701 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.661 |
MOD_GlcNHglycan | 361 | 366 | PF01048 | 0.626 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.661 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.623 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.426 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.327 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.570 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.615 |
MOD_GlcNHglycan | 579 | 583 | PF01048 | 0.487 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.770 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.615 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.486 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.718 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.524 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.645 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.667 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.592 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.487 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.711 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.619 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.579 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.529 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.744 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.594 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.502 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.511 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.638 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.509 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.458 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.717 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.529 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.542 |
MOD_NEK2_2 | 190 | 195 | PF00069 | 0.620 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.616 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.564 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.525 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.545 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.483 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.670 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.663 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.604 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.541 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.674 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.688 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.654 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.647 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.557 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.480 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.564 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.368 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.627 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.651 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.648 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.624 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.556 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.586 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.752 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.517 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.539 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.521 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6C8 | Leptomonas seymouri | 33% | 89% |
A0A3Q8IE95 | Leishmania donovani | 88% | 100% |
A4HAN7 | Leishmania braziliensis | 60% | 91% |
A4I9T0 | Leishmania infantum | 88% | 100% |
E9B4U1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 90% |