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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X349
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.414 |
DEG_APCC_DBOX_1 | 599 | 607 | PF00400 | 0.424 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.783 |
DOC_CDC14_PxL_1 | 370 | 378 | PF14671 | 0.400 |
DOC_MAPK_MEF2A_6 | 278 | 287 | PF00069 | 0.511 |
DOC_PP1_RVXF_1 | 481 | 488 | PF00149 | 0.497 |
DOC_PP4_FxxP_1 | 218 | 221 | PF00568 | 0.570 |
DOC_PP4_FxxP_1 | 444 | 447 | PF00568 | 0.411 |
DOC_SPAK_OSR1_1 | 182 | 186 | PF12202 | 0.569 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 170 | 174 | PF12436 | 0.486 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 389 | 396 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 519 | 529 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 564 | 568 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 600 | 609 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 619 | 627 | PF00244 | 0.295 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.474 |
LIG_Actin_WH2_2 | 579 | 594 | PF00022 | 0.580 |
LIG_BRCT_BRCA1_1 | 553 | 557 | PF00533 | 0.534 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.486 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.519 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.542 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.551 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.454 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.521 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.562 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.504 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.552 |
LIG_IRF3_LxIS_1 | 560 | 566 | PF10401 | 0.436 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 442 | 447 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 481 | 485 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.437 |
LIG_PCNA_PIPBox_1 | 304 | 313 | PF02747 | 0.560 |
LIG_PCNA_yPIPBox_3 | 262 | 270 | PF02747 | 0.522 |
LIG_PCNA_yPIPBox_3 | 380 | 389 | PF02747 | 0.503 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.690 |
LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.803 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.827 |
LIG_SH2_NCK_1 | 456 | 460 | PF00017 | 0.556 |
LIG_SH2_SRC | 456 | 459 | PF00017 | 0.553 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.820 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 553 | 557 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.602 |
LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.754 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.558 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.491 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.468 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 365 | 371 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 506 | 512 | PF11976 | 0.488 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.529 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.550 |
LIG_UBA3_1 | 166 | 174 | PF00899 | 0.457 |
LIG_UBA3_1 | 434 | 440 | PF00899 | 0.516 |
LIG_UBA3_1 | 493 | 501 | PF00899 | 0.538 |
LIG_WRC_WIRS_1 | 479 | 484 | PF05994 | 0.568 |
LIG_WW_3 | 50 | 54 | PF00397 | 0.754 |
LIG_WW_3 | 519 | 523 | PF00397 | 0.526 |
MOD_CDK_SPK_2 | 595 | 600 | PF00069 | 0.527 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.619 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.560 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.543 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.540 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.485 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.490 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.494 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.552 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.579 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.510 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.532 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.765 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.445 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.507 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.399 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.343 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.576 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.450 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.570 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.458 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.588 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.457 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.463 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.546 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.500 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.538 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.524 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.532 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.527 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.458 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.562 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.601 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.583 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.485 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.540 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.537 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.724 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.562 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.486 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.537 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.676 |
MOD_PKB_1 | 72 | 80 | PF00069 | 0.698 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.443 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.553 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.663 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.518 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.479 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.428 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.418 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.443 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.423 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.520 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.596 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 257 | 264 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 188 | 193 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_4 | 298 | 304 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.468 |
TRG_DiLeu_LyEn_5 | 188 | 193 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.696 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.495 |
TRG_NES_CRM1_1 | 279 | 293 | PF08389 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I169 | Leptomonas seymouri | 44% | 100% |
A0A0S4JB89 | Bodo saltans | 25% | 91% |
A0A1X0P251 | Trypanosomatidae | 38% | 100% |
A0A422P4U2 | Trypanosoma rangeli | 37% | 100% |
A4HI33 | Leishmania braziliensis | 80% | 100% |
A4I5A9 | Leishmania infantum | 100% | 100% |
C9ZQP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 91% |
E9B0K5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q7M7 | Leishmania major | 92% | 97% |