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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q4F4
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
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:0019538 | protein metabolic process | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 10 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
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:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 2 |
GO:0051540 | metal cluster binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.327 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.670 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.531 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.527 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.401 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.715 |
DOC_MAPK_RevD_3 | 98 | 114 | PF00069 | 0.344 |
DOC_PP1_RVXF_1 | 283 | 290 | PF00149 | 0.531 |
DOC_PP4_FxxP_1 | 69 | 72 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.547 |
DOC_USP7_MATH_2 | 254 | 260 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.669 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.344 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 305 | 315 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 337 | 345 | PF00244 | 0.683 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.408 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.527 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.452 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.553 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.753 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.499 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.594 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.667 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.474 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.342 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.429 |
LIG_GBD_Chelix_1 | 89 | 97 | PF00786 | 0.344 |
LIG_LIR_Apic_2 | 66 | 72 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 82 | 88 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 107 | 115 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 339 | 347 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 46 | 55 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.372 |
LIG_MYND_1 | 180 | 184 | PF01753 | 0.671 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.519 |
LIG_PTAP_UEV_1 | 242 | 247 | PF05743 | 0.588 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.485 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.729 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.635 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 258 | 265 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 312 | 319 | PF11976 | 0.541 |
LIG_SUMO_SIM_anti_2 | 7 | 12 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 258 | 267 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 312 | 319 | PF11976 | 0.554 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.644 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.471 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.444 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.716 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.664 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.474 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.653 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.662 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.765 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.675 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.522 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.363 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.592 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.599 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.625 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.710 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.756 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.429 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.430 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.491 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.560 |
MOD_GlcNHglycan | 328 | 332 | PF01048 | 0.357 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.696 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.758 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.747 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.743 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.444 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.632 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.481 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.683 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.495 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.590 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.728 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.705 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.644 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.447 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.580 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.442 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.490 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.629 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.600 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.403 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.429 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.531 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.527 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.597 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.674 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.697 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.500 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.571 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.344 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.704 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.667 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.601 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.483 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.444 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.569 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.551 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.662 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.600 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.406 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.411 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.405 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.751 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.483 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.728 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.659 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.356 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.344 |
MOD_SUMO_rev_2 | 216 | 224 | PF00179 | 0.439 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.688 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6M8 | Leptomonas seymouri | 63% | 90% |
A0A0S4J2M4 | Bodo saltans | 40% | 94% |
A0A3S7X6H5 | Leishmania donovani | 92% | 95% |
A4HL91 | Leishmania braziliensis | 76% | 99% |
A4I8R7 | Leishmania infantum | 92% | 95% |
D0A4Q8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B3N3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B2F6 | Trypanosoma cruzi | 53% | 94% |