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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005525 | GTP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.321 |
CLV_C14_Caspase3-7 | 502 | 506 | PF00656 | 0.799 |
CLV_C14_Caspase3-7 | 598 | 602 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.801 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 684 | 686 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 697 | 699 | PF00675 | 0.503 |
CLV_PCSK_FUR_1 | 242 | 246 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 699 | 701 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.541 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.665 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.490 |
DOC_CYCLIN_RxL_1 | 293 | 304 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 488 | 499 | PF00134 | 0.714 |
DOC_MAPK_gen_1 | 204 | 213 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 607 | 614 | PF00069 | 0.556 |
DOC_PP1_RVXF_1 | 119 | 126 | PF00149 | 0.490 |
DOC_PP1_RVXF_1 | 173 | 180 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.716 |
DOC_PP2B_LxvP_1 | 584 | 587 | PF13499 | 0.720 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.426 |
DOC_SPAK_OSR1_1 | 489 | 493 | PF12202 | 0.649 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 500 | 507 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 607 | 613 | PF00244 | 0.527 |
LIG_Actin_WH2_2 | 155 | 171 | PF00022 | 0.545 |
LIG_Actin_WH2_2 | 5 | 22 | PF00022 | 0.519 |
LIG_Actin_WH2_2 | 53 | 71 | PF00022 | 0.434 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 651 | 655 | PF00533 | 0.397 |
LIG_Clathr_ClatBox_1 | 132 | 136 | PF01394 | 0.561 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.622 |
LIG_eIF4E_1 | 308 | 314 | PF01652 | 0.480 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.490 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.505 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.514 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.448 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.661 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.810 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.604 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.561 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.803 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.527 |
LIG_IRF3_LxIS_1 | 8 | 15 | PF10401 | 0.567 |
LIG_LIR_Apic_2 | 328 | 332 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 347 | 352 | PF02991 | 0.259 |
LIG_LIR_Apic_2 | 710 | 715 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.361 |
LIG_NRBOX | 3 | 9 | PF00104 | 0.691 |
LIG_PCNA_PIPBox_1 | 268 | 277 | PF02747 | 0.482 |
LIG_PCNA_yPIPBox_3 | 356 | 370 | PF02747 | 0.486 |
LIG_Pex14_2 | 159 | 163 | PF04695 | 0.490 |
LIG_PTB_Apo_2 | 55 | 62 | PF02174 | 0.531 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.634 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.454 |
LIG_SH2_SRC | 329 | 332 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.539 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.472 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 130 | 137 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 130 | 137 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 608 | 613 | PF11976 | 0.557 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.609 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.602 |
LIG_TRAF2_1 | 643 | 646 | PF00917 | 0.614 |
LIG_TYR_ITIM | 14 | 19 | PF00017 | 0.624 |
LIG_WRC_WIRS_1 | 198 | 203 | PF05994 | 0.591 |
LIG_WRC_WIRS_1 | 346 | 351 | PF05994 | 0.421 |
MOD_CDC14_SPxK_1 | 541 | 544 | PF00782 | 0.513 |
MOD_CDK_SPxK_1 | 538 | 544 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 600 | 607 | PF00069 | 0.481 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.591 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.730 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.763 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.704 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.454 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.644 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.491 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.487 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.382 |
MOD_Cter_Amidation | 486 | 489 | PF01082 | 0.607 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.391 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.644 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.547 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.532 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.512 |
MOD_GlcNHglycan | 561 | 566 | PF01048 | 0.733 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.474 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.505 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.533 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.490 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.591 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.561 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.528 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.749 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.649 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.607 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.782 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.638 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.490 |
MOD_LATS_1 | 243 | 249 | PF00433 | 0.583 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.591 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.472 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.447 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.525 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.499 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.521 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.591 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.658 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.650 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.504 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.768 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.601 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.533 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.474 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.715 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.497 |
MOD_PK_1 | 701 | 707 | PF00069 | 0.582 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.598 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.598 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.784 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.704 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.582 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.492 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.511 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.552 |
MOD_Plk_1 | 701 | 707 | PF00069 | 0.582 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.591 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.695 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.423 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.733 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.515 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.490 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.490 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.561 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.744 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.562 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 364 | 371 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_2 | 269 | 275 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_3 | 196 | 202 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 491 | 496 | PF01217 | 0.714 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 676 | 679 | PF00400 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 493 | 498 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 743 | 747 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF47 | Leptomonas seymouri | 59% | 99% |
A0A1X0NRQ7 | Trypanosomatidae | 39% | 100% |
A0A3R7LAS2 | Trypanosoma rangeli | 43% | 100% |
A0A3S7X600 | Leishmania donovani | 91% | 100% |
A4HKU7 | Leishmania braziliensis | 78% | 98% |
A4I8C6 | Leishmania infantum | 91% | 100% |
Q4Q4X0 | Leishmania major | 90% | 100% |
V5BVC8 | Trypanosoma cruzi | 42% | 100% |