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: A0A3S7X6H5
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 | 277 | 281 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.572 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.465 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.510 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.344 |
DOC_MAPK_gen_1 | 330 | 339 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 24 | 32 | PF00069 | 0.575 |
DOC_MAPK_RevD_3 | 120 | 136 | PF00069 | 0.284 |
DOC_PP1_RVXF_1 | 305 | 312 | PF00149 | 0.490 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.481 |
DOC_USP7_MATH_2 | 276 | 282 | PF00917 | 0.502 |
DOC_USP7_UBL2_3 | 425 | 429 | PF12436 | 0.594 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.293 |
LIG_14-3-3_CanoR_1 | 327 | 337 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.716 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.504 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.312 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.398 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.528 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.783 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.397 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.533 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.657 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.615 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.432 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.284 |
LIG_GBD_Chelix_1 | 111 | 119 | PF00786 | 0.284 |
LIG_LIR_Apic_2 | 104 | 110 | PF02991 | 0.308 |
LIG_LIR_Apic_2 | 88 | 94 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 129 | 137 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 361 | 369 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.312 |
LIG_MYND_1 | 202 | 206 | PF01753 | 0.594 |
LIG_PTAP_UEV_1 | 264 | 269 | PF05743 | 0.506 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.684 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.386 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.576 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.519 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 280 | 287 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 334 | 341 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 280 | 289 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 334 | 341 | PF11976 | 0.523 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.585 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.329 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.400 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.695 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.432 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.616 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.658 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.595 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.574 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.655 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.397 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.533 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.578 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.556 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.562 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.634 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.664 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.395 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.434 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.497 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.273 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.461 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.769 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.715 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.502 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.674 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.428 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.620 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.555 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.457 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.577 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.657 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.698 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.652 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.336 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.512 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.346 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.353 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.447 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.447 |
MOD_NEK2_2 | 325 | 330 | PF00069 | 0.490 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.585 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.687 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.459 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.467 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.657 |
MOD_PKB_1 | 2 | 10 | PF00069 | 0.540 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.289 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.598 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.400 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.313 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.442 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.524 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.530 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.651 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.400 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.284 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.756 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.681 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.627 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.773 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.687 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.293 |
MOD_SUMO_rev_2 | 238 | 246 | PF00179 | 0.381 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.680 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 43 | 45 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M8 | Leptomonas seymouri | 63% | 95% |
A0A0S4J2M4 | Bodo saltans | 40% | 99% |
A4HL91 | Leishmania braziliensis | 75% | 100% |
A4I8R7 | Leishmania infantum | 100% | 100% |
D0A4Q8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B3N3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q4F4 | Leishmania major | 92% | 100% |
V5B2F6 | Trypanosoma cruzi | 52% | 99% |