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:0005643 | nuclear pore | 3 | 2 |
GO:0031080 | nuclear pore outer ring | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QCG3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.645 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.555 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.667 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.561 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.441 |
DOC_CKS1_1 | 340 | 345 | PF01111 | 0.563 |
DOC_MAPK_gen_1 | 111 | 117 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 33 | 43 | PF00069 | 0.525 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.395 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.526 |
LIG_Actin_WH2_2 | 252 | 267 | PF00022 | 0.503 |
LIG_BIR_III_4 | 359 | 363 | PF00653 | 0.520 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.614 |
LIG_EH1_1 | 232 | 240 | PF00400 | 0.524 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.444 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.409 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.240 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.469 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.659 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.547 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.666 |
LIG_LIR_Apic_2 | 222 | 228 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 429 | 435 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.498 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.419 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.650 |
LIG_SH2_PTP2 | 87 | 90 | PF00017 | 0.492 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.492 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.502 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.577 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.468 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.474 |
LIG_Sin3_3 | 74 | 81 | PF02671 | 0.456 |
LIG_SUMO_SIM_anti_2 | 246 | 251 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 73 | 80 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 113 | 122 | PF11976 | 0.555 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.433 |
LIG_TRFH_1 | 7 | 11 | PF08558 | 0.650 |
LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.407 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.639 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.434 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.628 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.523 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.574 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.495 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.551 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.669 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.572 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.659 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.608 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.568 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.525 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.541 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.488 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.567 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.520 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.734 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.503 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.505 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.668 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.728 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.511 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.538 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.598 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.438 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.598 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.529 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.560 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.427 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.399 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.369 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.706 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.496 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.542 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.678 |
MOD_PKA_1 | 317 | 323 | PF00069 | 0.586 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.558 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.533 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.548 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.512 |
MOD_PKB_1 | 33 | 41 | PF00069 | 0.538 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.473 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.516 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.419 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.432 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.549 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.649 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.491 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.553 |
TRG_DiLeu_BaEn_4 | 236 | 242 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 285 | 290 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P853 | Leptomonas seymouri | 54% | 88% |
A0A1X0NY38 | Trypanosomatidae | 29% | 100% |
A0A3Q8IDW0 | Leishmania donovani | 96% | 100% |
A0A422NBK7 | Trypanosoma rangeli | 31% | 100% |
A4HBP9 | Leishmania braziliensis | 85% | 100% |
A4HZ51 | Leishmania infantum | 96% | 100% |
D0A1Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AV19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BQ65 | Trypanosoma cruzi | 28% | 100% |