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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q5I4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.754 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.540 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.736 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.706 |
DOC_CYCLIN_RxL_1 | 153 | 162 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 331 | 337 | PF00134 | 0.621 |
DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 220 | 229 | PF00069 | 0.493 |
DOC_PP4_FxxP_1 | 397 | 400 | PF00568 | 0.636 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.796 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.513 |
LIG_APCC_ABBA_1 | 169 | 174 | PF00400 | 0.588 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.559 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.653 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.650 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.747 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.473 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.759 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.542 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.710 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.614 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.704 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.546 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.782 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 439 | 443 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.623 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.612 |
LIG_SH2_STAT3 | 411 | 414 | PF00017 | 0.615 |
LIG_SH2_STAT3 | 489 | 492 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.612 |
LIG_SH3_1 | 387 | 393 | PF00018 | 0.699 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.717 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.722 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.623 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.704 |
LIG_SUMO_SIM_par_1 | 482 | 487 | PF11976 | 0.665 |
LIG_TYR_ITIM | 507 | 512 | PF00017 | 0.630 |
MOD_CDK_SPxxK_3 | 285 | 292 | PF00069 | 0.628 |
MOD_CDK_SPxxK_3 | 448 | 455 | PF00069 | 0.706 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.691 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.649 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.636 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.706 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.583 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.668 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.612 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.617 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.431 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.652 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.656 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.669 |
MOD_Cter_Amidation | 537 | 540 | PF01082 | 0.689 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.693 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.388 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.561 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.677 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.682 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.627 |
MOD_GlcNHglycan | 456 | 460 | PF01048 | 0.724 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.696 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.723 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.660 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.608 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.692 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.644 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.671 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.725 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.614 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.654 |
MOD_LATS_1 | 218 | 224 | PF00433 | 0.538 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.719 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.376 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.715 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.447 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.629 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.642 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.499 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.546 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.605 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.561 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.604 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.705 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.467 |
MOD_OFUCOSY | 217 | 224 | PF10250 | 0.567 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.711 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.621 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.702 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.360 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.685 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.654 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.658 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.696 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.472 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.639 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.565 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.644 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.649 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.639 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.674 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.707 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.635 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.730 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.541 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.623 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.637 |
TRG_ER_diArg_1 | 539 | 541 | PF00400 | 0.746 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMP7 | Leptomonas seymouri | 53% | 100% |
A0A1X0NUL4 | Trypanosomatidae | 33% | 87% |
A0A3S7X5C4 | Leishmania donovani | 94% | 100% |
A4HK79 | Leishmania braziliensis | 74% | 100% |
A4I7R4 | Leishmania infantum | 94% | 100% |
E9B2M2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |