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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031390 | Ctf18 RFC-like complex | 3 | 5 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0140513 | nuclear protein-containing complex | 2 | 5 |
Related structures:
AlphaFold database: A4H4N4
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 5 |
GO:0007062 | sister chromatid cohesion | 3 | 5 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016043 | cellular component organization | 3 | 5 |
GO:0022402 | cell cycle process | 2 | 5 |
GO:0051276 | chromosome organization | 5 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 5 |
GO:1903047 | mitotic cell cycle process | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.629 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.703 |
CLV_PCSK_PC7_1 | 39 | 45 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.501 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.500 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.540 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.495 |
DOC_CYCLIN_RxL_1 | 220 | 230 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.520 |
DOC_MAPK_gen_1 | 153 | 160 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 153 | 162 | PF00069 | 0.613 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 128 | 138 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 338 | 345 | PF00244 | 0.511 |
LIG_AP2alpha_1 | 279 | 283 | PF02296 | 0.629 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.417 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.518 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.533 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.498 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.415 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.453 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.627 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.681 |
LIG_FXI_DFP_1 | 280 | 284 | PF00024 | 0.473 |
LIG_LIR_Apic_2 | 190 | 194 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.478 |
LIG_PCNA_PIPBox_1 | 272 | 281 | PF02747 | 0.449 |
LIG_PCNA_yPIPBox_3 | 359 | 367 | PF02747 | 0.313 |
LIG_Pex14_2 | 191 | 195 | PF04695 | 0.520 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.629 |
LIG_REV1ctd_RIR_1 | 147 | 158 | PF16727 | 0.491 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.418 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.308 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.666 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.486 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.697 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 68 | 74 | PF11976 | 0.507 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.489 |
LIG_UBA3_1 | 15 | 21 | PF00899 | 0.550 |
MOD_CDK_SPK_2 | 311 | 316 | PF00069 | 0.525 |
MOD_CDK_SPxK_1 | 199 | 205 | PF00069 | 0.441 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.662 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.582 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.615 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.688 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.701 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.597 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.523 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.614 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.676 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.574 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.462 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.362 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.647 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.548 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.560 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.605 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.460 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.640 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.617 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.411 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.638 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.648 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.573 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.756 |
MOD_GlcNHglycan | 94 | 98 | PF01048 | 0.574 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.746 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.594 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.617 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.636 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.675 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.570 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.591 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.773 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.600 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.642 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.623 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.494 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.524 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.543 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.463 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.411 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.603 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.422 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.599 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.468 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.612 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.468 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.367 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.446 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.677 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.674 |
MOD_PKB_1 | 292 | 300 | PF00069 | 0.537 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.614 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.524 |
MOD_Plk_2-3 | 85 | 91 | PF00069 | 0.500 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.530 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.446 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.570 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.681 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.616 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.407 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.714 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.441 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.572 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.581 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.616 |
TRG_NES_CRM1_1 | 271 | 284 | PF08389 | 0.454 |
TRG_NLS_MonoExtC_3 | 206 | 211 | PF00514 | 0.544 |
TRG_NLS_MonoExtN_4 | 205 | 211 | PF00514 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 207 | 212 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I714 | Leptomonas seymouri | 41% | 100% |
A0A3S7WPI0 | Leishmania donovani | 61% | 94% |
A4HSW0 | Leishmania infantum | 63% | 95% |
E9AKU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 94% |
Q4QJ09 | Leishmania major | 62% | 100% |