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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
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 | 10 |
Related structures:
AlphaFold database: Q4QAG1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.744 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.409 |
CLV_PCSK_FUR_1 | 127 | 131 | PF00082 | 0.386 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.323 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.623 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 302 | 311 | PF00069 | 0.503 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.690 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 370 | 377 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 458 | 468 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.678 |
LIG_Actin_WH2_2 | 300 | 317 | PF00022 | 0.542 |
LIG_AP2alpha_2 | 274 | 276 | PF02296 | 0.551 |
LIG_APCC_ABBA_1 | 273 | 278 | PF00400 | 0.560 |
LIG_CaM_IQ_9 | 119 | 135 | PF13499 | 0.619 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.670 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.583 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.683 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.558 |
LIG_LIR_Apic_2 | 32 | 36 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 241 | 251 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 328 | 334 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 53 | 59 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.632 |
LIG_Pex14_1 | 108 | 112 | PF04695 | 0.581 |
LIG_Pex14_2 | 343 | 347 | PF04695 | 0.250 |
LIG_RPA_C_Fungi | 427 | 439 | PF08784 | 0.556 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.575 |
LIG_SH3_5 | 266 | 270 | PF00018 | 0.529 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.461 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.494 |
LIG_TRFH_1 | 148 | 152 | PF08558 | 0.521 |
LIG_TRFH_1 | 271 | 275 | PF08558 | 0.508 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.509 |
LIG_UBA3_1 | 353 | 358 | PF00899 | 0.478 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.623 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.502 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.405 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.581 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.496 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.637 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.660 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.592 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.775 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.606 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.640 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.516 |
MOD_GlcNHglycan | 16 | 20 | PF01048 | 0.658 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.512 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.271 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.289 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.289 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.523 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.554 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.453 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.349 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.573 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.657 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.577 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.595 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.271 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.271 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.452 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.708 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.696 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.563 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.421 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.286 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.271 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.279 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.356 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.234 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.678 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.423 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.332 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.612 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.431 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.685 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.758 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.650 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.372 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.634 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.574 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.271 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.271 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.449 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.405 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.275 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.264 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.241 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.581 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.516 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.749 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.655 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.514 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.657 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.510 |
TRG_NLS_Bipartite_1 | 113 | 130 | PF00514 | 0.494 |
TRG_NLS_MonoExtC_3 | 125 | 130 | PF00514 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 52 | 56 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U8 | Leptomonas seymouri | 64% | 99% |
A0A0S4JPE5 | Bodo saltans | 43% | 100% |
A0A1X0NW21 | Trypanosomatidae | 52% | 100% |
A0A3S7WYL2 | Leishmania donovani | 95% | 100% |
A4HDN0 | Leishmania braziliensis | 84% | 100% |
C9ZWD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AH77 | Leishmania infantum | 95% | 100% |
E9AX15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5DBL9 | Trypanosoma cruzi | 47% | 100% |