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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QGF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.749 |
CLV_PCSK_FUR_1 | 144 | 148 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.378 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.378 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.583 |
DEG_SCF_FBW7_1 | 316 | 322 | PF00400 | 0.590 |
DOC_CDC14_PxL_1 | 372 | 380 | PF14671 | 0.554 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.531 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.662 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.639 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.559 |
DOC_CKS1_1 | 305 | 310 | PF01111 | 0.719 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.458 |
DOC_CYCLIN_yClb3_PxF_3 | 412 | 420 | PF00134 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 378 | 384 | PF00134 | 0.538 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.612 |
DOC_PP1_RVXF_1 | 422 | 429 | PF00149 | 0.562 |
DOC_PP1_RVXF_1 | 431 | 437 | PF00149 | 0.471 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.745 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 428 | 431 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.612 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 163 | 171 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 223 | 227 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 362 | 372 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.757 |
LIG_14-3-3_CterR_2 | 435 | 438 | PF00244 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.604 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.535 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.535 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.703 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.517 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.497 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.505 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.573 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.574 |
LIG_LIR_Apic_2 | 427 | 431 | PF02991 | 0.737 |
LIG_LIR_Gen_1 | 241 | 251 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.384 |
LIG_MYND_3 | 103 | 107 | PF01753 | 0.581 |
LIG_NRBOX | 31 | 37 | PF00104 | 0.483 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.610 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.585 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.491 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.459 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.566 |
LIG_SH2_SRC | 73 | 76 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.514 |
LIG_SH3_2 | 119 | 124 | PF14604 | 0.662 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.635 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.585 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.549 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.564 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.519 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.513 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.497 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.531 |
LIG_SUMO_SIM_par_1 | 133 | 139 | PF11976 | 0.654 |
LIG_SUMO_SIM_par_1 | 28 | 37 | PF11976 | 0.506 |
LIG_WW_3 | 121 | 125 | PF00397 | 0.665 |
MOD_CDC14_SPxK_1 | 204 | 207 | PF00782 | 0.815 |
MOD_CDC14_SPxK_1 | 430 | 433 | PF00782 | 0.609 |
MOD_CDK_SPK_2 | 139 | 144 | PF00069 | 0.629 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.560 |
MOD_CDK_SPK_2 | 277 | 282 | PF00069 | 0.552 |
MOD_CDK_SPK_2 | 315 | 320 | PF00069 | 0.596 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 201 | 207 | PF00069 | 0.633 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.642 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.643 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.526 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.573 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.665 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.595 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.629 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.669 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.695 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.591 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.665 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.588 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.663 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.620 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.549 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.637 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.579 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.650 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.586 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.777 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.593 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.588 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.664 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.662 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.535 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.688 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.577 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.500 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.492 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.502 |
MOD_LATS_1 | 213 | 219 | PF00433 | 0.544 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.377 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.668 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.757 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.497 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.440 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.409 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.588 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.800 |
MOD_PK_1 | 147 | 153 | PF00069 | 0.588 |
MOD_PK_1 | 406 | 412 | PF00069 | 0.573 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.548 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.676 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.660 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.708 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.613 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.640 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.801 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.700 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.621 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.562 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.618 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.706 |
MOD_PKB_1 | 130 | 138 | PF00069 | 0.612 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.568 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.627 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.573 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.668 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.613 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.547 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.688 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.681 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.710 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.651 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.674 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.645 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.564 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.655 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.568 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.523 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.612 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 192 | 201 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 83 | 90 | PF00179 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F0 | Leptomonas seymouri | 50% | 91% |
A0A3R7KKI7 | Trypanosoma rangeli | 31% | 97% |
A0A3S7WS94 | Leishmania donovani | 85% | 100% |
C9ZI49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 94% |
E9AGJ7 | Leishmania infantum | 85% | 100% |
E9AIN1 | Leishmania braziliensis | 63% | 100% |
E9AP34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |