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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HL91
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 10 |
GO:0022607 | cellular component assembly | 4 | 10 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005506 | iron ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0051536 | iron-sulfur cluster binding | 3 | 10 |
GO:0051540 | metal cluster binding | 2 | 10 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.491 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.187 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.477 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.476 |
DOC_CKS1_1 | 53 | 58 | PF01111 | 0.338 |
DOC_MAPK_gen_1 | 313 | 322 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.586 |
DOC_MAPK_RevD_3 | 99 | 115 | PF00069 | 0.279 |
DOC_PP1_RVXF_1 | 288 | 295 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 386 | 392 | PF00149 | 0.486 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.572 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.279 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.200 |
LIG_deltaCOP1_diTrp_1 | 223 | 229 | PF00928 | 0.353 |
LIG_EH1_1 | 228 | 236 | PF00400 | 0.344 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.387 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.540 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.694 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.437 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.591 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.279 |
LIG_GBD_Chelix_1 | 90 | 98 | PF00786 | 0.279 |
LIG_LIR_Apic_2 | 83 | 89 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 109 | 118 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 344 | 352 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.448 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.463 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.659 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.200 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.347 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 263 | 270 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 263 | 272 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 317 | 324 | PF11976 | 0.527 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.392 |
MOD_CDK_SPxK_1 | 40 | 46 | PF00069 | 0.393 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.410 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.489 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.612 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.638 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.533 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.541 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.624 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.329 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.586 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.542 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.592 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.624 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.525 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.628 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.584 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.351 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.452 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.414 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.479 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.579 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.620 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.565 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.422 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.552 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.526 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.524 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.475 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.594 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.451 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.573 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.567 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.752 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.636 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.519 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.324 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.357 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.689 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.389 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.467 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.433 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.571 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.715 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.340 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.486 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.439 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.544 |
MOD_PK_1 | 414 | 420 | PF00069 | 0.482 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.627 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.488 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.541 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.645 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.608 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.279 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.616 |
MOD_Plk_2-3 | 372 | 378 | PF00069 | 0.482 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.446 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.492 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.624 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.525 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.395 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.395 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.554 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.621 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.521 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.340 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 223 | 229 | PF00179 | 0.360 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.655 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.635 |
TRG_NES_CRM1_1 | 209 | 223 | PF08389 | 0.314 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M8 | Leptomonas seymouri | 60% | 91% |
A0A0S4J2M4 | Bodo saltans | 42% | 95% |
A0A3S7X6H5 | Leishmania donovani | 75% | 96% |
A4I8R7 | Leishmania infantum | 75% | 96% |
D0A4Q8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9B3N3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q4F4 | Leishmania major | 76% | 99% |
V5B2F6 | Trypanosoma cruzi | 50% | 95% |