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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A4HC42
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0000976 | transcription cis-regulatory region binding | 5 | 1 |
GO:0001067 | transcription regulatory region nucleic acid binding | 4 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 508 | 510 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.405 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.558 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.308 |
DEG_SCF_FBW7_2 | 246 | 253 | PF00400 | 0.524 |
DEG_SCF_FBW7_2 | 315 | 322 | PF00400 | 0.716 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.523 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.517 |
DOC_MAPK_gen_1 | 379 | 390 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 94 | 102 | PF00069 | 0.541 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.680 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.381 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 557 | 561 | PF12436 | 0.736 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 210 | 217 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 39 | 46 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 447 | 454 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 535 | 542 | PF00244 | 0.659 |
LIG_Actin_WH2_2 | 339 | 356 | PF00022 | 0.522 |
LIG_Actin_WH2_2 | 51 | 66 | PF00022 | 0.484 |
LIG_AP2alpha_2 | 214 | 216 | PF02296 | 0.555 |
LIG_APCC_ABBA_1 | 326 | 331 | PF00400 | 0.510 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
LIG_deltaCOP1_diTrp_1 | 458 | 462 | PF00928 | 0.697 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.490 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.419 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.707 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.550 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.470 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.722 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.345 |
LIG_Integrin_RGD_1 | 456 | 458 | PF01839 | 0.475 |
LIG_Integrin_RGD_1 | 526 | 528 | PF01839 | 0.743 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.414 |
LIG_LIR_Apic_2 | 214 | 220 | PF02991 | 0.356 |
LIG_LIR_Apic_2 | 48 | 52 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 477 | 484 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.642 |
LIG_MYND_1 | 309 | 313 | PF01753 | 0.629 |
LIG_PTAP_UEV_1 | 132 | 137 | PF05743 | 0.435 |
LIG_PTB_Apo_2 | 68 | 75 | PF02174 | 0.341 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.463 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.372 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.735 |
LIG_SH2_SRC | 329 | 332 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.687 |
LIG_SH3_2 | 185 | 190 | PF14604 | 0.498 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.387 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.380 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.603 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.612 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.652 |
LIG_SUMO_SIM_par_1 | 78 | 86 | PF11976 | 0.603 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.522 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.338 |
LIG_TRFH_1 | 176 | 180 | PF08558 | 0.495 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.713 |
LIG_UBA3_1 | 150 | 158 | PF00899 | 0.390 |
LIG_UBA3_1 | 286 | 295 | PF00899 | 0.537 |
LIG_WW_3 | 523 | 527 | PF00397 | 0.482 |
MOD_CDK_SPK_2 | 575 | 580 | PF00069 | 0.704 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.424 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.706 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.696 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.705 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.607 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.595 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.457 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.546 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.460 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.520 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.725 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.317 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.676 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.709 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.624 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.671 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.708 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.580 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.471 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.480 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.662 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.632 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.504 |
MOD_LATS_1 | 37 | 43 | PF00433 | 0.509 |
MOD_N-GLC_2 | 205 | 207 | PF02516 | 0.495 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.512 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.502 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.656 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.718 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.641 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.639 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.526 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.390 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.473 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.720 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.719 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.636 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.644 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.599 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.555 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.669 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.496 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.316 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.687 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.754 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.599 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.526 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.545 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.596 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.534 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.586 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.586 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.604 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.559 |
MOD_SUMO_for_1 | 560 | 563 | PF00179 | 0.742 |
MOD_SUMO_rev_2 | 292 | 300 | PF00179 | 0.601 |
TRG_DiLeu_BaEn_2 | 280 | 286 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.694 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.526 |
TRG_NLS_Bipartite_1 | 189 | 205 | PF00514 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWK4 | Leptomonas seymouri | 68% | 99% |
A0A0S4IP20 | Bodo saltans | 28% | 74% |
A0A1X0NGG7 | Trypanosomatidae | 40% | 100% |
A0A3S5H6A1 | Leishmania donovani | 84% | 100% |
A0A3S7WQF9 | Leishmania donovani | 86% | 100% |
A0A422NFU0 | Trypanosoma rangeli | 39% | 100% |
C9ZPG2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AG88 | Leishmania infantum | 86% | 100% |
E9AMJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q32NQ8 | Xenopus laevis | 23% | 77% |
Q4QI41 | Leishmania major | 85% | 98% |
V5DAD1 | Trypanosoma cruzi | 41% | 100% |