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: E9B3N3
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 | 116 | 120 | PF00656 | 0.264 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.681 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.476 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.470 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.338 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.579 |
DOC_MAPK_RevD_3 | 98 | 114 | PF00069 | 0.279 |
DOC_PP1_RVXF_1 | 283 | 290 | PF00149 | 0.493 |
DOC_PP4_FxxP_1 | 69 | 72 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.565 |
DOC_USP7_MATH_2 | 254 | 260 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.279 |
LIG_14-3-3_CanoR_1 | 305 | 315 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 337 | 345 | PF00244 | 0.576 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.312 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.390 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.540 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.714 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.439 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.547 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.622 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.429 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.279 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.374 |
LIG_GBD_Chelix_1 | 89 | 97 | PF00786 | 0.279 |
LIG_LIR_Apic_2 | 66 | 72 | PF02991 | 0.374 |
LIG_LIR_Apic_2 | 82 | 88 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 107 | 115 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 339 | 347 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 46 | 55 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.328 |
LIG_MYND_1 | 180 | 184 | PF01753 | 0.572 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.464 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.347 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.671 |
LIG_SH3_CIN85_PxpxPR_1 | 166 | 171 | PF14604 | 0.467 |
LIG_SUMO_SIM_anti_2 | 258 | 267 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 312 | 319 | PF11976 | 0.498 |
LIG_SUMO_SIM_anti_2 | 7 | 12 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 258 | 267 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 312 | 319 | PF11976 | 0.527 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.609 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.410 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.480 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.670 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.438 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.690 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.515 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.643 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.660 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.354 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.606 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.580 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.573 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.566 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.628 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.374 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.351 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.455 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.448 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.638 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.576 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.655 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.665 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.422 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.527 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.573 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.481 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.632 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.451 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.553 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.619 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.664 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.395 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.467 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.704 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.340 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.372 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.486 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.443 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.567 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.668 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.488 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.666 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.515 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.279 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.647 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.384 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.446 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.513 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.523 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.638 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.513 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.395 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.395 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.395 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.540 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.746 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.543 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.588 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.647 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.340 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 216 | 224 | PF00179 | 0.371 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.280 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.643 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M8 | Leptomonas seymouri | 64% | 90% |
A0A0S4J2M4 | Bodo saltans | 40% | 94% |
A0A3S7X6H5 | Leishmania donovani | 90% | 95% |
A4HL91 | Leishmania braziliensis | 75% | 100% |
A4I8R7 | Leishmania infantum | 90% | 95% |
D0A4Q8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
Q4Q4F4 | Leishmania major | 91% | 100% |
V5B2F6 | Trypanosoma cruzi | 49% | 94% |